US 4,028,334 AGrant

Piperidine Derivatives

Issue Date:1977-06-07

•19 Claims

Abstract

New piperidine derivatives of 1,3-pyrimidine and 1,3,5-triazine are used as stabilizers for organic materials, especially for polymers.

Metadata

Assignee

Ciba-Geigy Corporation

Inventors

Alexander Michael Chalmers
James Jack
Barry Cook

Application Information

Application Number:US 6172202

Filing Date:1975-09-26

Priority Date:1973-04-11

Art Unit:141

Classifications

IPC:

C07D23900C08K 534

Field of Search:

26045.8 N;45.8 NT;256.4 C;256.4 R;256.5 R

Patent Drawings

This patent does not have any drawings.

Description

Example 1

To 28.2 parts of 2,2,6,6-tetramethylpiperidin-4-ol in 200 parts of dry xyleneware added in portions 4.2 parts of sodium. This mixture was heated at reflux for 18 hours and then cooled. 10.1 parts of cyanuric chloride were added in portions and the mixture brought to a reflux temperature for 1 hour. Evaporation to dryness under reduced pressure was followed by extraction with petroleum ether (b.p. 60.degree.-80.degree. C.) using a Soxhlet extractor apparatus. Evaporation in vacuo gave the desired product contaminated with 2,2,6,6-tetramethylpiperidin-4-ol. Sublimation in vacuo removed this contaminant and the residual colourless solid was crystallised from petroleum ether (b.p. 60.degree.-80.degree. C.) to yield 23.7 parts of 2,4,6-tris[2',2',6',6'-tetramethylpiperidinyl-4'-oxy]-1,3,5-triazine of melting point 198.degree.-200' C. This material gave the following elemental analysis by weight:

Example 2

38 parts of polypropylene were homogenised with 0.76 part of n-octadecyl-.beta.-(4'-hydroxy-3',5'-di-t-butylphenyl) propionate in a kneading machine over a period of 3 minutes. 0.19 part of the product of Example 1 was then added and homogenisation continued for another 7 minutes.

The homogenised mixture was removed from the kneader and pressed to a thickness of from 2 to 3 mm. in a press.

9 parts of the polypropylene mixture were then charged into a second press in which the press-plates were protected by aluminum foil having a thickness of 0.1 mm. The press was closed and, for 2 minutes, no pressure was applied. The pressure was then increased up to a maximum of 12 tons and this pressure held for 6 minutes, the temperature of the press being 260.degree. C. The pressure was released and the material (0.3 mm thick) was cooled under running water.

This material was cut from 3 to 5 pieces of 35.times. 35 mm section and re-charged to the press. The press was closed and no pressure was applied for 2 minutes. Over another 2 minutes the pressure was increased to 8 tons, the press temperature being 260.degree. C. This pressure was maintained for 2 minutes and then the pressure released. The polypropylene foil of 0.1 mm thickness was removed and tempered immediately in a circulating air oven maintained at 150.degree. C. over a period of 60 minutes.

A section measuring 44.times. 100 mm was separated from the 0.1 mm tempered polypropylene foil and exposed to light irradiation in a fademeter device consisting of a circular bank of 28 alternate sunlight and blacklight lamps. The sunlight lamps were 2 feet long, 20-watt fluorescent lamps characterised by a peak emission of 3,000 Angstrom units; the blacklight lamps were 2 feet long, 40-watt ultraviolet lamps characterized by a peak emission of 3,500 Angstrom units. The sample was rotated concentrically about the bank of lamps so that the radiation therefrom was uniformly distributed over the section under test.

The exposed sample was examined periodically and the time at which the sample reached 50% of the initial elongation was noted.

Example 3

1000 Parts by weight of unstabilised polypropylene powder were thoroughly dry-blended with 1 part by weight of n-octadecyl-.beta.-(4'-hydroxy-3', 5'-di-t-butylphenyl) propionate and 2 parts of the product of Example 1. The dry-blend was extruded at cylinder tempertures of from 180.degree. to 220.degree. C. and the resulting strand was granulated. The stabilised formulation so obtained was melt-spun and stretched under the following conditions:

The multifilament obtained was mounted on a sample holder of a Xenotest 150 apparatus (Quarzlampen GmbH) using white cardboard as backing. In intervals of 200 hours of exposure time, 5 fibre samples are measured for their retained tensile strength. The data obtained are plotted against exposure time and the exposure time to give 50% loss of original tensile strength is derived from the graph. This value is taken as the failure time.

The data are shown in the following Table II which also includes data relating to a control experiment omitting the product of Example 1.

Example 4

18.5 Parts of cyanuric chloride were slurried in 600 parts of water and treated with 31.4 parts of 4-amino-2,2,6,6-tetramethylpiperidine. 8 Parts of sodium hydroxide in 20 parts of water were then carefully added and the suspension stirred at room temperature for thirty minutes. The suspension was then heated at 90.degree. C. for 16 hours and allowed to cool. 39.5 Parts of a colourless solid, 2-chloro-4,6-bis(2',2',6' , 6'-tetramethylpiperidinyl-4'-amino)-1,3,5-triazine were separated by filtration, washed with water and dried in vacuo. This material of melting point 277.degree.-278.degree. C., showed the following elemental analysis by weight:

Example 5

12 Parts of the material obtained in Example 4 were warmed in a solution comprising 920 parts of ethanol and 190 parts of water. 9 Parts of 4-amino-2,2,6,6-tetra-methylpiperidine were added and the solution heated at reflux for 16 hours. The solution was then evaporated to dryness and treated with 200 parts of water. Filtration afforded 14.0 parts of a colourless solid 2,4,6-tris[2',2',6' ,6'-tetramethyl piperidinyl-4'-amino]-1,3,5-triazine monohydrate which was purified by Soxhlet extraction of the impurities with petroleum ether (of boiling range 60.degree.-80.degree. C.) The residual material of melting point 213.degree.-215.degree. C., gave the following elemental analysis by weight:

Prolonged heating in vacuo of this compound afforded the anhydrous material of melting point 217.degree.-219.degree. C.

Example 6

8.19 Parts of the material prepared in Example 1 were dissolved in in 60 parts of isopropanol and 9 parts of methyl iodide added with water cooling. After 120 hours a solid was separated by filtration and washed with diethyl ether. The solid was dissolved in the minimum amount of water and sodium carbonate added until the solution was basic. Chloroform extraction afforded 2,4,6-tris [1',2' ,2' ,6' ,6'-pentamethylpiperidinyl-4'-oxyl]-1,3,5-triazine. This material was crystallized from a 1:1 mixture of chloroform and ethanol to give a colourless solid of melting point 245.degree.-247.degree. C. which gave the following elemental analysis by weight.

Example 7

25.8 Parts of 4-hydroxyl-2,2,6,6-tetramethylpiperidin-1 -oxyl and 8.4 parts of potassium hydroxide were dissolved in 500 parts of water. 9.2 parts of cyanuric chloride were carefully added and the solution heated at reflux for 2 hours. 5 Parts of a solid were filtered off and washed with 20 parts of water followed by 20 parts of boiling petroleum ether (boiling range 80.degree.-100.degree. C.). After drying this material 2,4,6-tris[1'-oxyl-2', ,2' ,6' ,6'-tetramethylpiperidinyl-4'-oxy]-1,3,5-triazine, gave a melting point of 192.degree.-194.degree. C. and the following elemental analysis by weight:

Example 8

14.75 Parts of cyanuric chloride were carefully added to a mixture of 25 parts of 2,2,6,6,-tetra methyl piperidin-4-ol and 13.5 parts of sodium bicarbonate in 250 parts of water. The mixture was stirred and heated to give a clear solution. After 6 hours a colourless precipitate had been produced which was filtered after cooling. The solid was washed three times with 100 parts of water and dried in a vacuum oven to give 13.5 parts of 2-chloro-4,6-bis(2' ,2' ,6' ,6'-tetra methyl piperidinyl-4'-oxy)-1,3,5-triazine monohydrate. This material, of melting point 225.degree.-226.degree. C., showed the following elemental analysis by weight:

Example 9

To 10.4 parts of 4-hydroxy-2,2,6,6-tetra methyl piperidin-1-oxyl in 160 parts of dry benzene were added, in portions, 1.38 parts of sodium. This mixture was heated at reflux for 18 hours and then cooled. 3.7 Parts of cyanuric chloride were added with care and the mixture heated at reflux for 18 hours. On cooling the inorganic salt was removed by filtration and the filtrate evaporated in vacuo. Sublimation in vacuo of the residual solid removed unreacted 4-hydroxy-2,2,6,6-tetra methyl piperidin-1-oxyl and the residue was recrystallized three times from absolute ethanol to yield 2-chloro-4,6-bis(1'-oxyl-2',2' ,6' ,6'-tetra methyl piperidinyl-4'-oxy)-1,3,5-triazine. This material had a melting point of 197.degree.-199.degree. C. and showed the following elemental analysis by weight:

Example 10

To 4.94 parts of 1-benzyl-2,2,6,6-tetra methyl piperidin-4-ol in 100 parts of xylene were added, in portions, 0.8 parts of sodium. This mixture was heated at reflux for 18 hours and then cooled. The excess sodium was removed and 1.2 parts of cyanuric chloride added with care. The mixture was stirred at reflux temperature for 3 hours. Evaporation of the solvent in vacuo afforded a solid which was Soxhlet extracted with petroleum ether (of boiling range 80.degree.-100.degree. C.) to give 1.7 parts of a pale yellow solid. Column chromatography on silica afforded 2,4,6-tri (1'-benzyl- 2',2' ,6' ,6'-tetra methyl piperidinyl-4'oxy)-1,3,5-triazine. This material had a melting point of 125.degree.-129.degree. C. and showed the required spectroscopic features (Infrared, Nuclear Magnetic Resonance Spectroscopy and Mass Spectrometry).

Example 11

4.8 Parts of 2-chloro-4,6-bis(2' ,2' ,6' ,6'-tetra methyl piperidin-4'-amino)-1,3,5-triazine were dissolved in a mixture of 300 parts of toluene and 200 parts tertiary butyl alcohol with warming. A solution of 4 parts of the sodium salt of 2,2,6,6-tetra methyl piperidin-4-ol in 40 parts toluene (as prepared in the above Examples) was added dropwise and the mixture heated at reflux for 18 hours. Evaporation of the solution and treatment of the residue with 15 parts of water afforded 4 parts of a colourless solid which was filtered and dried in vacuo. This material, 2,4-bis[2' ,2' ,6' ,6'-tetra methyl piperidinyl- 4'-amino]-6-[2",2" ,6" ,6"-tetra methyl piperidinyl-4"-oxy]-1,3,5-triazine, was crystallised from methanol and water to give a melting point of 186.5.degree.- 187.5.degree. C. and had the following elemental analysis by weight:

Example 12

4 Parts of 2,4,6-tris[2',2' ,6' ,6'-tetra methyl piperidin-4'-amino]-1,3,5-triazine in 100 parts of isopropanol at 5.degree. C. were treated with 6.4 parts of iodomethane. The mixture was allowed to stand at room temperature for 3 days. Evaporation in vacuo afforded a residue which was treated with saturated sodium carbonate. Filtration and drying in vacuo afforded a colourless solid which was shown by spectroscopic means to be a partially methylated material. This material was dissolved in 180 parts of isopropanol and treated with 4 parts of iodomethane. The mixture was allowed to stand at room temperature for 3 days. Evaporation in vacuo, followed by treatment with saturated sodium carbonate, afforded a colourless solid, 2,4,6-tris(1'2' ,2' ,6' ,6'-pentamethylpiperidinyl-4'-amino)-1,3,5-triazine, which was filtered and dried in vacuo. This material was column chromatographed on alumina and then recrystallised from methanol and water to give a melting point of 235.degree.-240.degree. C. The compound gave the following elemental analysis by weight:

Example 13

To 4.8 parts of 2-chloro-4,6-bis(2' ,2' ,6' ,6'-tetramethyl piperidinyl-4'-amino)-1,3,5-triazine in a mixture of 100 parts of ethanol and 20 parts of water were added 4 parts of 4-(.beta.-aminoethyl)-2,2,6,6-tetra methyl piperidine. The solution was stirred at reflux for 8 hours and then evaporated in vacuo. The residue was dissolved in 25 parts of chloroform and washed with 50 parts of water. The chloroform phase was dried and evaporated to yield 6.0 parts of a colourless solid of melting point 75.degree. C. This material was column chromatographed on alumina to give 2,4-bis(2' ,2' ,6' ,6'-tetra methyl piperidinyl-4'-amino)-6-(2" ,2" ,6" ,6"-tetra methyl piperidinyl-4"-ethylenamino)-1,3,5-triazine of melting point 96.degree.-99.degree. C. This substance showed the following elemental analysis by weight:

Example 14

To 3.94 parts of 1-allyl-2,2,6,6-tetramethyl piperidin-4-ol in 100 parts of toluene were added 0.8 parts of sodium. This mixture was heated at reflux for 18 hours and the excess sodium removed. 1.24 Parts of cyanuric chloride were added with care and the solution was stirred at reflux for 41/2 hours. The solvent was evaporated in vacuo yielding a residue which was column chromatographed on alumina to give 2-chloro-4,6-bis(1'-allyl-2' ,2' ,6' ,6'-tetra methyl piperidinyl-4'-oxy)-1,3,5-triazine of melting point 167.degree.-170.degree. C. This substance gave the following elemental analysis by weight:

Example 15

5.6 Parts by weight of 2 -(2',2' ,6' ,6'-tetra methyl piperidinyl-4')ethyl alcohol and 1.4 parts by weight of sodium were heated to reflux for 24 hours in 100 parts by volume of toluene. To the resulting solution were added over 20 minutes 1.8 parts by weight of cyanuric chloride in 30 parts by volume of toluene, and the reflux continued for 18 hours. The toluene was then removed by distillation under reduced pressure and the solid suspended in water, this was extracted with ether (3.times. 50 parts by volume), and the combined extracts dried over magnesium sulphate. The ether was removed by distillation and the residue was triturated with petroleum ether to give a solid which was collected by filtration, dissolved in 20 parts by volume of ethyl alcohol and reprecipitated by the addition of 100 parts by volume of water.

Thus was obtained pure 2,4,6-tris[2' ,2' ,6' ,6'-tetramethyl piperidinyl-4'-ethylenoxy]1,3,5-triazine, melting at 104.degree.-6.degree. and having the following elemental analysis by weight:

Example 16

1.8 Parts by weight of cyanuric chloride and 11.0 parts by weight of 2-(2',2',6',6'-tetramethylpiperidinyl-4') ethylamine were heated at 160.degree. with stirring for 4 hrs. The resulting mass was cooled and the oil decanted off, this was diluted with 100 parts by volume of water and allowed to stand at room temperature for 24 hours. A solid precipitate was filtered, dried, and recrystallised from ethyl acetate (50 parts by volume) to give pure 2,4,6-tris[ 2',2',6',6'-tetramethylpiperidinyl-4'-ethylenamino] 1,3,5-triazine, melting at 169.degree. and having the following elemental analysis by weight:-

Example 17

3.7 Parts of cyanuric chloride were stirred in a mixture of 120 parts of ethanol and 120 parts of water, the temperature being maintained at -15.degree. C. 3.12 Parts of 4-amino-2,2,6,6-tetramethyl piperidine were added whilst maintaining this temperature. After 2 hours, a colourless solid had been precipitated; this material was separated by filtration and dried in vacuo to yield 2,4-dichloro-6-(2',2',6',6'-tetramethyl piperidinyl -4'-amino)-1,3,5-triazine (4.2 parts) as the hydrochloric acid salt. This salt had a melting point of over 275.degree. C. and gave the following elemental analysis by weight:

Example 18

A solution of 7.4 parts by weight of 2-(2',2',6',6'-tetramethyl piperidinyl-4') ethyl amine in 20 parts by volume of toluene was added dropwise to a stirred solution of 1.85 parts by weight of cyanuric chloride in 80 parts by volume of toluene. The resulting suspension was stirred at room temperature for 24 hours, and the solid then collected by filtration and treated with a 10% solution of sodium hydroxide in water for a further 12 hours.

The resulting solid was collected by filtration, washed repeatedly with water until the aqueous washings were pH 6- 7, dried at 60.degree. C., and purified by reprecipitation from a chloroform solution by the addition of petroleum ether (boiling range 60.degree. - 80.degree. C.) to give 2-chloro-4,6-di [2',2',6',6'-tetramethylpiperidinyl-4'-ethylenamino]-1,3,5-triazine, melting at 168.degree. C. and having the following elemental analysis by weight:

Examples 19

38 Parts of polypropylene were homogenised with 0.076 parts of n-octadecyl-.beta. (4'-hydroxy-3',5'-t-butyl-phenyl) propionate in a kneading machine over a period of 3 minutes at 200.degree. C. 0.19 Part of the product of Example 5 was then added and homogenisation was continued for another 7 minutes.

This composition was compression moulded into films of 0.1 mm. thickness at 260.degree. C. for 6 minutes and the films so obtained were then quenched in cold water.

A section measuring 44.times. 100 mm. was separated from the 0.1 mm. annealed polypropylene foil and exposed to light irradiation in a fademeter device consisting of a circular bank of 28 alternate sunlight and blacklight lamps. The sunlight lamps were 2 feet long, 20-watt fluorescent lamps characterised by a peak emission of 3,100 Angstrom units; the blacklight lamps were 2 feet long, 20-watt ultra-violet lamps characterised by a peak emission of 3,500 Angstrom units.

The sample was rotated concentrically about the bank of lamps so that the radiation thereupon was uniformly distributed over the section under test.

The exposed sample was examined periodically and portions of it tested to determine the percentage elongation at break, the time (T) at which the sample reached 50% of the initial elongation at break being noted.

A similar test was carried out on a polypropylene sample containing no stabiliser of the invention.

The results obtained are set out in the following Table:

Example 20

5.6 parts of 2-ethylamino-4,6-dichloro-1,3,5-triazine was slurried in 300 parts of water and the mixture heated to a temperature of 55.degree. C. 4.8 parts of 4-amino-2,2,6,6-tetramethylpiperidine were then added followed by 30 parts of IN sodium hydroxide. The mixture was stirred at 55.degree. C. for six hours. A colourless solid was then filtered off and washed with 700 parts of warm water. 6.0 parts of 2-ethylamino-4-chloro-6-(2',2',6',6'-tetramethylpiperidinyl-4'-amino)-1,3, 5-triazine were obtained. This material had a melting point of 189.degree. to 191.degree. C. and gave the following elemental analysis by weight:

Example 21

Using identical conditions to Example 20, 6.2 parts of 2-isopropylamino-4,6-dichloro-1,3,5-triazine were reacted with 4.8 parts of 4-amino-2,2,6,6-tetramethylpiperidine to yield 7 parts of 2-isopropylamino-4-chloro-6-(2',2',6',6'-tetramethylpiperidinyl-4'-amino)- 1,3,5-triazine. This substance had a melting point of 174 to 176.degree. C. and gave the following elemental analysis by weight.

Example 22

Using identical conditions to Example 20, 6.7 parts of 2-n-octylthio-4,6-dichloro-1,3,5-triazine were reacted with 3.55 parts of 4-amino-2,2,6,6-tetramethylpiperidine to yield 9.1 parts of 2-n-octylthio-4-chloro-6-(2',2',6',6'-tetramethylpiperidinyl-4'-amino)-1,3 ,5-triazine. This material had a melting point of 79.degree. to 81.degree. C. and gave the following elemental analysis by weight:

Example 23

3.6 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol were heated with 0.6 parts of sodium to reflux temperature in toluene. After 16 hours the solution was cooled, the excess sodium removed and treated with 4.1 parts of 2-chloro-4,6-dimethylthio-1,3,5-triazine. The solution was heated at reflux temperature for 18 hours after which it was cooled and filtered free of sodium chloride. The solvent was evaporated under reduced pressure to yield a residue which was crystallised from petroleum ether (of boiling point 60.degree.-80.degree. C.). Two parts of 2,4-dimethylthio-6-[1',2',2',6',6'-pentamethylpiperidinyl-4'-oxy]-1,3,5-tr iazine were obtained which showed a melting point of 143.degree. to 145.degree. C. and gave the following elemental analysis by weight:

Example 24

2.4 parts of 2-chloro-4,6-bis-[2',2',6',6'-tetramethylpiperidinyl-4'-amino]-1,3,5-triaz ine were treated with 1.2 parts of isopropylamine in 40 parts of water. The solution was stirred at room temperature for 18 hours, at reflux temperature for four hours and then cooled and evaporated to yield 1.6 parts of material. This residue was treated with 10 parts of dilute sodium hydroxide and extracted twice with 50 parts of chloroform. After drying and removal of the solvent a semi-solid material was obtained which on addition of two parts of methanol yielded a colourless solid 2-isopropylamino-4,6-bis-[2',2',6',6'-tetramethylpiperidinyl-4'-amino]-1,3 ,5-triazine of melting point 120.degree. to 122.degree. C. It showed the following elemental analysis by weight:

Example 25

0.36 parts of sodium were added to 150 parts of ethanol and the solution treated with 6.6 parts of 2-chloro-4,6-bis-[2',2',6',6'-tetramethylpiperidinyl-4'-amino]-1,3,5-triaz ine. The mixture was stirred and heated at reflux for 16 hours after which the solution was cooled and filtered. Evaporation of the filtrate in vacuo afforded 6.6 parts of a colourless solid which was chromatographed on an alumina column to yield 2-ethoxy-4,6-bis-(2',2',6',6'-tetramethylpiperidinyl-4'-amino)-1,3,5-triaz ine. This material has a melting point of 189.degree. to 191.degree. C. and gave the following elemental analysis by weight:

Example 26

6.28 Parts of 4-amino-2,2,6,6-tetramethylpiperidine were dissolved in 100 parts of toluene and 4.1 parts of 2-chloro-4,6-di(methylthio)-1,3,5-triazine were carefully added. The solution was stirred at reflux temperature for 6 hours. 6 Parts of a solid were filtered off and dried. This material was treated with 30 parts of saturated sodium carbonate solution and extracted with 300 parts of chloroform. The organic extract was dried and evaporated to yield a colourless tacky solid. Column chromatography on alumina afforded pure 2-(2',2',6',6'-tetramethylpiperidinyl-4'-amino)-4,6-di(methylthio-1,3,5-tr iazine. This material was recrystallised from ethanol and had a melting point of 173.degree. to 175.degree. C. It showed the following elemental analysis by weight:

Example 27

1.4 Parts of sodium and 6.28 parts of 2,2,6,6-tetramethylpiperidin-4-ol was heated at reflux temperature for 24 hours in 100 parts of toluene. To this cooled solution was added 3.86 parts of 2-ethylamino-4,6-dichloro-1,3,5-triazine and the mixture heated at reflux for 2 hours. Evaporation of the solvent in vacuo afforded a material which was extracted with chloroform using a Soxhlet extractor. The extract was evaporated to yield a colourless solid which was chromatographed on an alumina column and then crystallised from ethyl acetate, to give pure 2-ethylamino-4,6-bis[2',2',6',6'-tetramethylpiperidinyl-4'-oxy]-1,3,5-tria zine which showed a melting point of 189.5.degree. to 190.5.degree. and the following elemental analysis by weight:

Example 28

3 Parts of 2,4-dichloro-6-(2',2',6',6',-tetramethylpiperidinyl-4'-amino)-1,3,5-triazi ne hydrochloric acid salt were dissolved in 400 parts of a 1:1 mixture of ethanol and water. 1.18 Parts of n-propylamine were added and the solution heated at reflux for 18 hours. Evaporation of the solvent afforded a colourless solid which was crystallised from the solvent mixture methanol/petroleum ether (of boiling range 60.degree.-80.degree.)/ethyl acetate to give pure 2-chloro-4-n-propylamino-6-(2',2',6',6'-tetramethylpiperidyl-4'-amino)-1,3 ,5-triazine hydrochloric acid salt of melting point greater than 270.degree. and which gave the following analysis by weight:

Example 29

A solution of 2.1 parts by weight of 2-chloro-4,6-di(methylthio)-1,3,5-triazine and 4.0 parts by weight of 2(1',2',2',6',6'-pentamethylpiperidinyl-4')-ethylamine in 50 parts by volume of toluene was heated at reflux for 4 hours. The toluene was then filtered and removed by distillation under reduced pressure to give a residual oil, which by trituration with petroleum ether (boiling range 40.degree.-60.degree.) gave a white solid. Recrystallisation from 25 parts by volume of petroleum ether (60.degree.-80.degree.) gave pure 2-(1',2',2',6',6'-pentamethylpiperidinyl-4'-ethylenamino)-4,6-di(methylthi o-1,3,5-triazine, melting at 119.degree. and having the following elemental analysis by weight:

Example 30

1.5 Parts of 2-chloro-4,6-bis[2',2',6',6-tetramethylpiperidinyl-4' -amino]-1,3,5-triazine were dissolved in 130 parts of an ethanol/water (5:1) mixture and 4 parts of dimethylamine in ethanol solution (33%) added. The mixture was heated in a rocking autoclave at a temperature of 100.degree. C. and a pressure of 20 atmospheres nitrogen for 24 hours. The solution was filtered and the filtrate evaporated in vacuo to yield a pale brown solid. Charcoal treatment of this material removed the colour and the product was Soxhlet extracted with petroleum ether (of boiling range 60.degree.-80.degree.) for 24 hours to yield 2-dimethylamino-4,6-bis[2',2',6',6-tetramethylpiperidinyl-4'-amino]-1,3,5- triazine monohydrate as a colourless solid. It showed a melting point of 230.degree. to 233.degree. C., a molecular weight of 432 by mass spectrometry and the following elemental analysis by weight:

Example 31

3 Parts of 2-chloro-4,6-bis[2',2',6',6' -tetramethylpiperidin-yl-4' -amino]-1,3,5-triazine were dissolved in a mixture of 225 parts of ethanol and 46 parts of water with stirring and heating. 1.26 Parts of morpholine were added and the solution heated at reflux for 24 hours. The solution was then evaporated in vacuo and 50 parts of water added. After stirring for 30 minutes the solution was filtered and the filtered material treated with 50 parts of saturated sodium carbonate solution and extracted with 200 parts of chloroform. The extract was dried and evaporated in vacuo to yield 2-morpholino-4,6-bis[2',2',6',6'-tetramethylpiperidinyl-4'-amino]-1,3,5-tr iazine dihydrate as a colourless solid of melting point 179.degree.-181.degree. C. This solid had a molecular weight of 474 by mass spectrometry and showed the following elemental analysis by weight:

Example 32

2.2 Parts of 2-chloro-4,6-bis[2',2',6',6'-tetramethylpiperidinyl-4'-amino]-1,3,5-triazi ne and 1.07 parts of benzylamine were heated at reflux in a mixture of 150 parts of ethanol and 30 parts of water for 18 hours. An evaporation of the solvent, a material was obtained which was chromatographed on an Alumina column. Crystallisation from water gave 2-benzylamino-4,6-bis[2',2',6',6'-tetramethylpiperidinyl-4'-amino]-1,3,5-t riazine monohydrate as a colourless solid of melting point 98.degree. to 100.degree. C. It gave the following elemental analysis by weight:

Example 33

2 Parts of 2-chloro-4,6-bis[2',2',6',6'-tetramethylpiperidinyl-4'-oxy]-1,3,5-triazine and 2.48 parts of 4-amino-2,2,6,6-tetramethylpiperidine were heated at reflux with a mixture of 42 parts ethanol and 20 parts water for 18 hours. A pure colourless solid was filtered from the solution which had a melting point of over 280.degree. C. and a molecular weight of 406 by mass spectrometry. This material was the hydrochloric acid salt of 2-amino-4,6-bis[2',2',6',6'-tetramethylpiperidinyl-4'-amino]-1,3,5-triazin e and showed the following elemental analysis by weight:

Example 34

3.6 Parts of 2,4,6-trichloropyrimidine were dissolved in a mixture of 12 parts of water and 20 parts of dioxane and the solution stirred and cooled to 5.degree. C. 3 Parts of 4-amino-2,2,6,6-tetramethylpiperidine were then added slowly maintaining a temperature of below 10.degree. C. 0.8 Parts of sodium hydroxide in 2 parts of water were added and the solution stirred at room temperature for 1 hour. 4.4 Parts of 4-amino-2,2,6,6-tetramethylpiperidine were then added followed by 0.8 parts sodium hydroxide in 2 parts of water. The resultant solution was then stirred at reflux temperature for 18 hours. A solid material was filtered off, treated with 100 parts of saturated sodium carbonate solution and extracted with 200 parts of chloroform. The extract was dried and evaporated to yield a solid, 6-chloro-2,4-bis[2',2',6',6-tetramethylpiperidinyl-4'-amino]-1,3-pyrimidin e monohydrate which was recrystallised from chloroform/petroleum ether (of boiling range 40-60.degree.) to give a melting point of 198.degree. to 199.5.degree. C. and the following elemental analysis by weight:

Claims

We claim:

1. A compound of the formula ##STR27## and salts thereof, wherein Z' is a group having the formula: ##STR28## wherein R.sub.1 and R.sub.2 are the same or different and each is a straight or branched alkyl having from 1 to 12 carbon atoms or R.sub.1 and R.sub.2 form, together with the ring carbon atom to which they are bound, a cycloalkyl having from 5 to 12 carbon atoms; ##STR29## R.sub.7 is hydrogen, a straight- or branched alkyl having from 1 to 20 carbon atoms or an aralkyl having from 7 to 12 carbon atoms; Y is oxygen, hydrogen, a straight- or branched alkyl having from 1 to 20 carbon atoms, an alkenyl or alkynyl having from 3 to 12 carbon atoms, an aralkyl group having from 7 to 12 carbon atoms or the group ##STR30## wherein R.sub.8 is hydrogen, or a methyl or phenyl; n is zero or 1; and A is --CH.sub.2 --, or the group ##STR31## wherein R.sub.9 is a hydrogen or an alkyl having from 1 to 20 carbon atoms; Z" and Z'" are the same or different and each is a piperidine group of formula II as hereinbefore defined, a halogen atom, a substituted amino group having the formula: ##STR32## wherein R.sub.3 and R.sub.4 are the same or different and each is hydrogen, a straight or branched alkyl having from 1 to 20 carbon atoms, a cycloalkyl having from 5 to 12 carbon atoms, an aryl which is unsubstituted or substituted with one or more alkyl groups and having a total of from 6 to 18 carbon atoms or an aralkyl having from 7 to 12 carbon atoms, or R.sub.3 and R.sub.4, together with the nitrogen atom to which they are bound, form a heterocyclic group having 5 to 7 ring atoms; or Z" and Z'" are a hydroxy or an ether group having the formula: wherein R.sub.5 is hydrogen, a straight or branched chain alkyl having from 1 to 20 carbon atoms, a cycloalkyl having from 5 to 12 carbon atoms, an aryl which is unsubstituted or substituted by one or more alkyl groups and having a total of 6 to 18 carbon atoms, or an aralkyl having from 7 to 12 carbon atoms; or Z" and Z'" are a thiol or thio ether group having the formula: wherein R.sub.6 is hydrogen, a straight or branched alkyl having from 1 to 20 carbon atoms or a cycloalkyl having from 5 to 12 carbon atoms.

2. A compound of claim 1 wherein X is --O-- or --NH--, n is zero, R.sub.1 and R.sub.2 are each methyl and Y is hydrogen or methyl.

3. A compound of claim 2 wherein Z" and Z'" are each independently a halogen atom or a piperidine group of formula II.

4. The compound of claim 1 which is 6-chloro-2,4-bis(2',2'-6',6'-tetramethylpiperidinyl-4'-amido)-1,3-pyrimidi ne monohydrate.

5. A composition of matter stabilized against ultraviolet and heat deterioration which comprises a synthetic organic polymer normally subject to deterioration containing from 0.1% to 2% by weight of the polymer of a stabilizing compound having the formula ##STR33## and salts thereof, wherein U is --CH-- or --N--, Z' is a group having the formula: ##STR34## wherein R.sub.1 and R.sub.2 are the same or different and each is a straight or branched alkyl having from 1 to 12 carbon atoms or R.sub.1 and R.sub.2 form, together with the ring carbon atom to which they are bound, a cycloalkyl having from 5 to 12 carbon atoms; X is an --O--, ##STR35## wherein R.sub.7 is hydrogen, a straight- or branched alkyl having from 1 to 20 carbon atoms or an aralkyl having from 7 to 12 carbon atoms; Y is oxygen, hydrogen, a straight- or branched alkyl having from 1 to 20 carbon atoms, an alkenyl or alkynyl having from 3 to 12 carbon atoms, an aralkyl having from 7 to 12 carbon atoms or the group ##STR36## wherein R.sub.8 is hydrogen, or a methyl or phenyl; n is 0 or 1; and A is --CH.sub.2 --, or the group ##STR37## wherein R.sub.9 is a hydrogen or an alkyl residue having from 1 to 20 carbon atoms; Z" and Z'" are the same or different and each is a piperidine group of formula II as hereinbefore defined, a halogen atom, a substituted amino group having the formula: ##STR38## wherein R.sub.3 and R.sub.4 are the same or different and each is hydrogen, a straight or branched alkyl having from 1 to 20 carbon atoms, a cycloalkyl having from 5 to 12 carbon atoms, an aryl which is unsubstituted or substituted with one or more alkyl groups and having a total of from 6 to 18 carbon atoms or an aralkyl having from 7 to 12 carbon atoms, or R.sub.3 and R.sub.4, together with the nitrogen atoms to which they are bound, form a heterocyclic group having 5 to 7 ring atoms; or Z" and Z'" are a hydroxy or an ether group having the formula: wherein R.sub.5 is hydrogen, a straight or branched chain alkyl having from 1 to 20 carbon atoms, a cycloalkyl having from 5 to 12 carbon atoms, an aryl which is unsubstituted or substituted by one or more alkyl groups and having a total of 6 to 18 carbon atoms, or an aralkyl having from 7 to 12 carbon atoms; or Z" and Z'" are a thiol or thio ether group having the formula: wherein R.sub.6 is hydrogen, a straight or branched alkyl residue having from 1 to 20 carbon atoms or a cycloalkyl residue having from 5 to 12 carbon atoms.

6. A composition according to claim 5 wherein the stabilizer has the formula ##STR39## and salts thereof, wherein D', D", and D'" are the same or different and each is halogen or a group of the formula: ##STR40## wherein R'.sub.1 and R'.sub.2 are the same or different and each is a straight or branched alkyl having from 1 to 12 carbon atoms, or R'.sub.1 and R'.sub.2, together with the carbon atom to which they are bound, form a cycloalkyl having from 5 to 12 carbon atoms, X' is --O--, --S-- or R'.sub.7 group wherein R'.sub.7 is hydrogen, an alkyl having from 1 to 12 carbon atoms or an aralkyl having from 7 to 12 carbon atoms, Y' is oxygen, hydrogen, an alkyl having from 1 to 12 carbon atoms, an alkenyl or alkynyl having from 3 to 12 carbon atoms, an aralkyl having from 7 to 12 carbon atoms or the group: ##STR41## wherein R'.sub.8 is hydrogen, or methyl or phenyl, N' is zero or 1 and A' is --CH.sub.2 --, --CH.sub.2 CH.sub.2 -- or ##STR42## wherein R'.sub.9 is an alkyl having from 1 to 12 carbon atoms, with the proviso that at least one of D', D" and D'" is not a halogen atom.

7. A composition according to claim 6 wherein D', D" and D'" are the same or different piperidine group IIA.

8. A composition according to claim 6, wherein X is --O-- or --NH, n is zero, R.sub.1 and R.sub.2 are each methyl and Y is hydrogen or methyl.

9. A composition according to claim 5 wherein the stabilizer has the formula: ##STR43## and salts thereof, wherein R".sub.1 and R".sub.2 are the same or different and each is a straight or branched chain alkyl having from 1 to 12 carbon atoms or R".sub.1 and R".sub.2, together with the carbon atom to which they are each bound, form a cycloalkyl group having from 5 to 12 carbon atoms, and Y" is hydrogen, a straight or branched chain alkyl group having from 1 to 12 carbon atoms, an alkenyl group having from 3 to 12 carbon atoms or an aralkyl group having from 7 to 12 carbon atoms.

10. A composition according to claim 9, wherein R".sub.1 and R".sub.2 are each methyl and Y" is hydrogen or methyl.

11. A composition of claim 5 wherein the organic polymer is a polyolefine.

12. A composition according to claim 11 wherein the stabilizer is 2,4,6-tris-(2',2',6',6'-tetramethylpiperidinyl-4'-oxy)-1,3,5-triazine.

13. A composition according to claim 11 wherein the stabilizer is 2,4,6--tris-(2',2',6',6'-tetramethylpiperidinyl-4'-amino)-1,3,5-triazine.

14. A composition according to claim 11 wherein the stabilizer is 2,4,6-tris-(1'-2'2',6',6'-pentamethylpiperidinyl-4'-oxy)-1,3,5-triazine.

15. A composition according to claim 11 wherein the stabilizer is 2,4,6-tris-(1'-oxyl-2',2',6',6'-tetramethylpiperidinyl-4'-oxy)-1,3,5-triaz ine.

16. A composition according to claim 11 wherein the stabilizer is 2-chloro-4,6-bis-(1'-oxyl-2',2',6',6'-tetramethylpiperidinyl-4'-oxy)-1,3,5 -triazine.

17. A composition of matter stabilized against ultraviolet and heat deterioration which comprises a synthetic organic polymer normally subject to deterioration containing from 0.1% to 2% by weight of the polymer of a stabilizing compound according to claim 1.

18. A composition as claimed in claim 17, wherein the polymer is polyolefine.

19. A composition as claimed in claim 18, wherein the stabilizer is 6-chloro-2,4-bis(2',2',6',6'-tetramethylpiperidinyl-4'-amido)-1,3-pyrimidi ne monohydrate.

Patent Citations (4)

Patent	Date	Inventor
US3723428	1973-03-01	Song
US3850877	1974-11-01	Cook
US3887516	1975-06-01	Song
US3887517	1975-06-01	Murayama et al.

Description