US 4,122,084 AGrant
Disulfides of Amino-Substituted Mercaptopyridine-1-Oxide
Issue Date:1978-10-24
•6 Claims
Abstract
Disulfide of amino-containing mercaptopyridine-1-oxide having particular utility as antimicrobial agents per se and in skin cleansing detergent compositions, shampoos, hair dressings, disinfectants, preservatives and the like.
Metadata
Assignee
- Colgate-Palmolive Company
Inventor
- Miriam L. Douglass
Application Information
Application Number:US 7916124
Filing Date:1977-04-27
Priority Date:1975-11-06
Art Unit:121
Classifications
IPC:
C07D21302
Field of Search:
260294.8 J
Patent Drawings
This patent does not have any drawings.
Description
The following examples are given to illustrate specific preferred embodiments of this invention. Clearly, the invention is not limited thereto. All temperatures are given in degrees Centigrade and all parts are by weight, unless otherwise indicated.
EXAMPLE 1
Preparation of 2-acetamido-6-mercaptopyridine-1-oxide
Step 1: 20 g (0.116 mole) of 2-amino-6-bromopyridine was dissolved in 140 ml. acetic anhydride and heated at 70.degree. C for 45 minutes. 2-Acetamido-6-bromopyridine was isolated by filtration as white flakes, m.p.=159.2.degree.-160.0.degree. C, in 68% yield. The excess acetic anhydride present in the reaction mixture was hydrolyzed by the addition of 300 ml. water to the filtrate; the reaction mixture was agitated and an additional 27% yield of 2-acetamido-6-bromopyridine was collected by filtration, giving a 95% yield of reaction product, 2-acetamido-6-bromopyridine which was recrystallized from benzene.
Elemental Analysis:
Infrared characteristics (IR), absorption wave length in microns: N--H; 3.13, 3.31; C.dbd.O; 6.02.
Step 2: 23.4 gms (0.109 mole) of 2-acetamido-6-bromopyridine was dissolved in 200 ml. of glacial acetic acid containing 27.6 ml (0.218 mole) of 7.9M peracetic acid and the solution was heated at 70.degree. C for 2 hours and at 55.degree. C for 19 hours. The reaction mixture was diluted with 1600 ml water and the solution was then concentrated in vacuo to 550 ml. 8.6% of unreacted-2-acetamido-6-bromopyridine was removed by filtration. The solvent was evaporated from the filtrate giving an 83% yield of impure 2-acetamido-6-bromopyridine-1-oxide which was purified by treatment with activated charcoal to remove the yellow impurity and subsequently recrystallized from 2-propanol. A second recrystallization from 2-propanol gave fine white needles, m.p=180.0.degree.-180.5.degree. C.
Elemental Analysis:
Step 3: 2 gms (0.0087 mole) of 2-acetamido-6-bromopyridine-1-oxide was suspended in 35 ml (0.035 mole) of 1M aqueous sodium hydrosulfide and 30 ml of ethanol and agitated at 60.degree. C for 5 hours and at room temperature one night. Concentrated hydrochloric acid was added dropwise to the cold yellow solution and the precipitated solid filtered, giving a 79% yield of 2-acetamido-6-mercaptopyridine-1-oxide. This impure product was purified by recrystallization from 2-propanol and hot filtration to remove a small amount of contaminating sulfur to give pale yellow crystals, m.p.=172.8.degree.-173.5.degree. C.
EXAMPLE 2
Preparation of the zinc salt of 2-acetamido-6-mercaptopyridine-1-oxide: 0.50M aqueous sodium hydroxide was added to 0.251g (0.00136 mole) of 2-acetamido-6-mercaptopyridine-1-oxide, as prepared in Example 1, in 3 ml of water until a pH of 5 was obtained by said solution. 4.0 ml (0.0080 mole) of 0.20M aqueous zinc nitrate was added to said solution, whereby the zinc salt of 2-acetamido-6-mercaptopyridine-1-oxide precipitated immediately. Upon filtration, an 84% yield of the zinc salt was obtained.
EXAMPLE 3
Preparation of the sodium salt of 2-ethoxycarbonylamino-6-mercaptopyridine-1-oxide
Step 1: 10.0 g (0.0578 mole) of 2-amino-6-bromopyridine was dissolved in 40 ml dry pyridine and 6.4 ml (0.067 mole) of ethyl chloroformate was added dropwise while the solution was stirred and cooled in an ice-bath to maintain the reaction temperature at 15.degree.-18.degree. C. After 4 hours at room temperature, the reaction mixture was poured into 150 ml of ice water and kept at 0.degree. C overnight. Impure 2-ethoxycarbonylamino-6-bromopyridine was obtained by filtration and subsequently recrystallized from 2:1 methanol-water solution, giving an 88% yield of white solid, m.p.=70.2.degree.-71.0.degree. C.
Step 2: A suspension of 2.0 g (0.00816 mole) of 2-ethoxycarbonylamino-6-bromopyridine in 10 ml of glacial acetic acid containing 1.3 ml (0.0102 mole) of 7.9M peracetic acid was heated at 70.degree. C for 17 hours. The light yellow reaction mixture was cooled and diluted with 70 ml water and 8.5% unreacted 2-ethoxycarbonylamino-6-bromopyridine was removed by filtration. The solution was concentrated in vacuo and the resultant viscous liquid was dissolved in chloroform and extracted with saturated aqueous sodium carbonate and dried. The chloroform was removed in vacuo, leaving a yellow liquid which crystallized on standing. Impure 2-ethoxycarbonylamino-6-bromopyridine-1-oxide was recrystallized from cyclohexane, giving a 97.4% yield of off-white powder, m.p.=66.0.degree.-67.5.degree. C. A second recrystallization from cyclohexane raised the melting point to 66.5.degree.-67.5.degree. C.
Step 3: A suspension of 1.3 g (0.0050 mole) of 2-ethoxycarbonylamino-6-bromopyridine- 1-oxide in 17 ml (0.017 mole) of 1M aqueous sodium hydrosulfide and 10 ml of ethanol was stirred at 65.degree. C for 2 hours. The reaction mixture was cooled and filtered, giving a 78% yield of the sodium salt of 2-ethoxycarbonylamino-6-mercaptopyridine-1-oxide, a white product which was recrystallized from aqueous ethanol.
EXAMPLE 4
Preparation of the sodium salt of 2-ethoxycarbonylamino-6-mercaptopyridine-1-oxide:
The procedure of Example 3 was repeated except that Step 2 relating to the oxidation to the pyridine-oxide was changed, whereby a chloroform solution of 2-ethoxycarbonylamino-6-bromopyridine was treated with m-chloroperbenzoic acid as the oxidizing agent for 9 days at room temperature, giving a 62% yield of 2-ethoxycarbonylamino-6-bromopyridine-1-oxide.
EXAMPLE 5
Preparation of the zinc salt of 2-ethoxycarbonylamino-6-mercaptopyridine-1-oxide:
0.236 g (0.00100 mole) of the sodium salt of 2-ethoxycarbonylamino-6-mercaptopyridine-1-oxide as prepared in Example 3 or Example 4 was dissolved in 15 ml water and 2.6 ml (0.00052 mole) of 0.20M aqueous zinc nitrate was added dropwise while stirring the solution. A white solid precipitated immediately and was isolated by filtration giving a 68% yield of the zinc salt of 2-ethoxycarbonylamino-6-mercaptopyridine-1-oxide.
EXAMPLE 6
Preparation of Bis[2-(6-ethoxycarbonylamino-1-oxopyridyl)] disulfide: 0.20 g (0.0084 mole) of the sodium salt of 2-ethoxycarbonylamino-6-mercaptopyridine-1-oxide prepared in accordance with either Example 3 or Example 4, was suspended in 8 ml water and stirred while adding 0.1M aqueous potassum triiodide until the yellow color of excess triiodide persisted. An 89% yield of impure bis[2-(6-ethoxycarbonylamino-1-oxopyridyl)] disulfide precipitated and was recrystallized from acetonitrile to give a white solid, mp=186.0.degree.-186.5.degree. C.
EXAMPLE 7
Preparation of Bis[2-(6-acetamido-1-oxopyridyl)-disulfide]
A suspension of 0.40g (0.00217 mole) of 2-acetamido-6-mercaptopyridine-1-oxide, prepared as in Example 1, in 5 ml of water acidified to a pH of 2 with 2M aqueous hydrochloric acid, was stirred while adding: 0.1M aqueous potassium triiodide until a permanent yellow color of triiodide was evident. The reaction product was filtered, giving a 70% yield of a tan product which was purified by recrystallization from glacial acetic acid, m.p.=249.0.degree.-250.0.degree. C.
EXAMPLE 8
Preparation of 2-ethoxycarbonylamino-6-benzylthiopyridine-1-oxide
A suspension of 1.0 g (0.0038 mole) of 2-ethoxycarbonylamino-6-bromopyridine-1-oxide, as prepared in Step 2 of Example 3, in 25 ml of methanol containing equivalent amounts of benzyl mercaptan and sodium methoxide, is heated under reflux for 2 hours. The reaction mixture is diluted with 150 ml water and the impure product is collected by filtration. Recrystallization from ethyl acetate-cyclohexane gave white needles having a m.p. of 139.8.degree.-140.2.degree. C.
From the elemental analysis and infrared spectral examination of the substituted amino-mercaptopyridine-oxide compounds and the intermediates thereof, the structure of each compound with above examples has been ascertained.
EXAMPLE 9
In lieu of the sodium salt of 2-ethoxycarbonylamino-6-mercaptopyridine-oxide, other salts such as the zinc salt, or the acylamino mercapto compound per se may be utilized. Similarly beneficial results are also obtainable by utilizing other shampoo formulations, based on nonionic or cationic detergents or other of the previously mentioned synthetic detergents instead of the mentioned combination of anionic detergents. A similar result is noted when the shampoo is based on soluble higher fatty acid soap. Usually, for shampoo applications, the milder of the mentioned detergents will be selected, so as to avoid unduly drying or embrittling the hair.
10
Approximately three cubic centimeters per application is used in treating human hair and scalp. This treatment may be repeated daily over a period of weeks. The compositions are especially useful with respect to diminishing fungal and bacterial counts and are particularly effective against Pityrosporum ovale, the yeast most frequently associated with dandruff, even in the presence of the sebum normally found on the hair and scalp.
In place of the particular salts of 2-acetamido-6-mercaptopyridine-1-oxide of the above formulas, similar proportions, or variations in proportions within the ranges described in the specification, of other salts, e.g., the copper, nickel, chromium, trimethylcetyl ammonium, ammonium, alkanolamine and other such salts, may be employed to obtain substantially similar antimicrobial activities. It is noted that the bactericides are especially useful even in the normally oily environment of the scalp and hair and in the lipophilic phases of hairdressings.
Similar results are obtained when the mentioned bactericides are used in similar proportions in other cosmetics, e.g., hair setting compositions, "aerosol" hair sprays, hair dyes, skin creams, talcum powders and foot powders.
The invention has been described with respect to various illustrations and embodiments thereof. However, the invention is broader than the illustrations given and it will be evident to one of ordinary skill in the art that substitutes and equivalents may be employed within the inventive concept.
Claims
What is claimed is:
1. A disulfide of mercaptopyridine-1-oxide having the following structural formula: ##STR10## wherein R is selected from the group consisting of the acyl radical R.sub.o C.dbd.O and the alkoxycarbonyl radical R.sub.o --OC.dbd.O, where R.sub.o is a C.sub.1 -C.sub.6 alkyl, aryl selected from the class consisting of phenyl or naphthyl, or aralkyl, said alkyl portion having 1-6 carbons, or halobenzyl, the C.sub.1 -6 alkane sulfonyl radical, the aralkanesulfonyl radical, and the arenesulfonyl radical ArSO.sub.2 wherein the aryl radical may be substituted by a C.sub.1 -C.sub.6 alkyl, alkoxy and/or a halo-radical; R.sub.1, R.sub.2 and R.sub.3 are each independently selected from the group consisting of hydrogen, methyl, two of said terms may represent methoxy and the other hydrogen, and one of said terms may represent ethyl, n-butyl, methoxy, ethoxy, phenyl, bromophenyl, chlorophenyl, trichlorophenyl, naphthyl, chlorobenzyl, dichlorobenzyl or furyl and the other two terms represent hydrogen.
2. A compound according to claim 1, wherein R.sub.1, R.sub.2 and R.sub.3 are all hydrogen.
3. A compound according to claim 1, which is the disulfide of a 2-acylamino-6-mercaptopyridine-1-oxide.
4. A compound according to claim 1, which is the disulfide of a 2-alkoxycarbonylamino-6-mercaptopyridine1-oxide.
5. A compound according to claim 4, which is bis [2-(6-ethoxycarbonylamino-1-oxopyridyl)]disulfide.
6. A compound according to claim 3, which is bis[2-(6-acetamido-1-oxopyridyl)] disulfide.
Patent Citations (2)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US3890434 | 1975-06-01 | Weisse et al. | |
| US4053606 | 1977-10-01 | Shen et al. |