US 4,371,734 AGrant
Preparation of Thiazole Derivatives
Issue Date:1983-02-01
•4 Claims
Abstract
A process for the preparation of a thiazole derivative of the formula ##STR1## where R.sup.1 to R.sup.4 are organic radicals and R.sup.3 and R.sup.4 may also be hydrogen, by reacting a compound of the formula ##STR2## with a methylene-active compound of the formula ##STR3## in the presence of a base, and the thiazole derivative thus obtained.
Metadata
Assignee
- BASF Aktiengesellschaft
Inventor
- Guenther Seybold
Application Information
Application Number:US 145790&
Filing Date:1980-05-01
Priority Date:1978-01-17
Art Unit:122
Classifications
IPC:
C07D27720
Field of Search:
548544146;202;203;143;152;131367;300;133;135
Patent Drawings
This patent does not have any drawings.
Description
The present invention relates to a process for the preparation of tautomeric compounds of the general formulae IA and IB ##STR4## where
R.sup.1 and R.sup.2 are cyano, formyl, nitro, unsubstituted or substituted alkanoyl or aroyl, a carboxylic acid ester group, unsubstituted or substituted carbamyl or sulfamyl, alkylsulfonyl, arylsulfonyl or alkylsulfinyl,
R.sup.1 and R.sup.2 may also together be a cyclic radical and
R.sup.2 may also be aryl or hetaryl,
R.sup.3 and R.sup.4 are hydrogen, unsubstituted or substituted alkyl, aryl, hetaryl, a carboxylic acid ester group, alkanoyl or aroyl and
R.sup.3 and R.sup.4 may also together be a cyclic radical, wherein a compound of the formula II ##STR5## is reacted with a compound of the formula III ##STR6## in the presence of a base.
The invention also relates to novel thiazoles.
Examples of radicals R.sup.1 and R.sup.2 are C.sub.1 -C.sub.8 -alkanoyl, which is unsubstituted or substituted by, for example, chlorine, bromine or C.sub.1 -C.sub.4 -alkoxy, benzoyl which is unsubstituted or substituted by chlorine, bromine, methyl, ethyl, methoxy, ethoxy or cyano, naphthoyl, carboxylic acid ester groups derived from C.sub.1 -C.sub.8 -alkanols, C.sub.2 - to C.sub.8 -glycols or -glycol ethers or phenols, carbamoyl or sulfamoyl substituted by C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxyalkyl, cyclohexyl or phenyl, C.sub.1-C.sub.4 -alkylsulfonyl or C.sub.1 -C.sub.8 -alkylsulfinyl, phenylsulfonyl or phenylsulfinyl.
The same radicals may be mentioned as examples of R.sup.3 and R.sup.4 within the scope of the general definition.
Specific examples of radicals R.sup.1, in addition to those already mentioned, are: COCH.sub.3, COC.sub.2 H.sub.5, COC.sub.3 H.sub.7, COCH.sub.2 Cl, COCHCl.sub.2, COC.sub.6 H.sub.5, COC.sub.6 H.sub.4 Cl, COOCH.sub.3, COOC.sub.2 H.sub.5, COOC.sub.3 H.sub.7, COOC.sub.4 H.sub.9, COOC.sub.6 H.sub.5, COO(CH.sub.2).sub.3 OCH.sub.3, COO(CH.sub.2).sub.3 OC.sub.2 H.sub.5, CONHCH.sub.3, CONHC.sub.2 H.sub.5, CONHC.sub.3 H.sub.7, CONHC.sub.4 H.sub.9, CON(CH.sub.3).sub.2, CON(C.sub.2 H.sub.5).sub.2, CONH.sub.2, CONHC.sub.6 H.sub.5, ##STR7## as well as the corresponding sulfamoyl radicals, CH.sub.3 SO.sub.2, C.sub.2 H.sub.5 SO.sub.2, C.sub.4 H.sub.9 SO.sub.2 and CH.sub.3 SO.
R.sup.2 may be identical with R.sup.1, and in addition some specific examples of R.sup.2 are O.sub.2 N-C.sub.6 H.sub.4, NC-C.sub.6 H.sub.4, CH.sub.3 COC.sub.6 H.sub.4, ##STR8##
R.sup.1 and R.sup.2 together may also form a cyclic radical, for example ##STR9## where aryl is phenyl which is unsubstituted or substituted by, for example, chlorine, bromine, methyl, ethyl, methoxy or ethoxy.
Specific examples of radicals R.sup.3 and R.sup.4 are:
CH.sub.3, C.sub.2 H.sub.5, C.sub.3 H.sub.7, C.sub.4 H.sub.9, C.sub.5 H.sub.11, C.sub.6 H.sub.5, C.sub.6 H.sub.13, C.sub.7 H.sub.15, C.sub.1 - bis C.sub.4 -alkyl-OC.sub.6 H.sub.4, (C.sub.1 -C.sub.4 -alkyl).sub.2 OC.sub.6 H.sub.3, Cl-C.sub.6 H.sub.4 Cl.sub.2 C.sub.6 H.sub.3, BrC.sub.6 H.sub.4, Br.sub.2 C.sub.6 H.sub.3, C.sub.1 -C.sub.4 -alkyl- S-C.sub.6 H.sub.4, H.sub.5 C.sub.6 S-C.sub.6 H.sub.4, C.sub.1 -C.sub.4 -alkyl-CONHC.sub.6 H.sub.4, COOCH.sub.3, COOC.sub.2 H.sub.5, COOC.sub.3 H.sub.7, COOC.sub.4 H.sub.9, COC.sub.6 H.sub.5, COCH.sub.3 and CH.sub.2 COO-C.sub.1 -C.sub.4 -alkyl,
R.sup.3 and R.sup.4 together can also complete a ring, for example ##STR10##
Suitable bases for the reaction are, in principle, all basic compounds, eg. alkali metal compounds or alkaline earth metal compounds, amines and alcoholates.
Specific examples are hydroxides, eg. NaOH, KOH, Ca(OH).sub.2, Ba(OH).sub.2 and Mg(OH).sub.2, carbonates, eg. Na.sub.2 CO.sub.3, K.sub.2 CO.sub.3 and Li.sub.2 CO.sub.3, alcoholates, eg. NaOCH.sub.3, NaOC.sub.2 H.sub.5, KOH(CH.sub.3).sub.3 and KOCH.sub.3, and amines, eg. NH.sub.3, ethylamine, piperidine, pyrrolidine, N(CH.sub.3).sub.3, N(C.sub.2 H.sub.5).sub.3, N(C.sub.4 H.sub.9).sub.3, N(CH.sub.2 CH.sub.2 OH).sub.3, C.sub.6 H.sub.5 N(CH.sub.3).sub.2 and pyridine.
The reaction of the compounds II and III is advantageously carried out in a solvent. Examples of suitable solvents are hydrocarbons, alcohols, glycols, glycol ethers, amides, ethers, ketones and nitriles; the solvents may also be used as mixtures with water.
In some cases, the bases may also serve as solvents.
Specific examples of solvents are toluene, xylenes, chlorobenzene, methylene chloride, ethylene chloride, chloroform, methanol, ethanol, isopropanol, isobutanol, ethylene glycol, ethylene glycol monomethyl ether, monoethyl ether and monobutyl ether, dimethylformamide, dimethylacetamide, N-methylpyrrolidone, tetrahydrofuran, dioxane, acetone, methyl ethyl ketone, cyclohexanone, acetonitrile and dimethylsulfoxide.
Examples of preferred solvents are methanol, ethanol, isobutanol and dimethylformamide.
Details of how the reaction may be carried out are to be found in the Examples, where parts and percentages are by weight, unless stated otherwise.
The process according to the invention is of particular importance for the preparation of compounds of the formula Ia ##STR11## where
B.sup.1 and B.sup.2 are cyano, C.sub.1 -C.sub.4 -alkoxycarbonyl, C.sub.1 -C.sub.4 -alkanoyl, substituted carbamoyl or hetaryl and
B.sup.3 and B.sup.4 are unsubstituted or chlorine-, bromine-, C.sub.1 -C.sub.4 -alkoxy-, methyl-, acetylamino- or C.sub.1 -C.sub.4 -alkylmercapto-substituted phenyl, methyl or ethyl.
The compounds of the formula I are valuable intermediates, e.g. for the preparation of dyes, and many of them are novel.
Specific examples of dyes obtainable with the compounds of formula I are e.g. described in copending Application Ser. No. 920,638, now 4,239,894.
The invention hence also concerns, by way of novel products, the compounds of the formula IV ##STR12## where
X.sup.1 is cyano, nitro, unsubstituted or substituted carbamoyl or sulfamoyl, alkylsulfonyl, arylsulfonyl or alkylsulfinyl,
X.sup.2 is cyano, nitro, unsubstituted or substituted carbamoyl or sulfamoyl, alkylsulfonyl or alkylsulfinyl, a carboxylic acid ester group, aryl or hetaryl, and
X.sup.1 and X.sup.2 may also, together with the methine group, be a cyclic radical and
R.sup.3 and R.sup.4 have the stated meanings.
EXAMPLE 1
4-Phenyl-thiazolylmalodinitrile
33 parts of malodinitrile and 90 parts of phenacyl thiocyanate are introduced into 500 parts of alcohol. 46 parts of triethylamine are then added dropwise at 30.degree. C., whilst stirring, after which the reaction mixture is stirred at room temperature overnight. It is then diluted with 500 parts of H.sub.2 O and is rendered slightly acid with glacial acetic acid, and the product is filtered off; it is a finely crystalline powder. Yield: 112 parts=99.5%.
Melting point 255.degree. C. (with decomposition).
EXAMPLE 2
Methyl 4-phenylthiazolylcyanoacetate
90 parts of phenacyl thiocyanate are introduced into a mixture of 150 parts of DMF, 150 parts of triethylamine and 50 parts of methyl cyanoacetate. The mixture is then stirred for 4 hours at room temperature, after which it is introduced into water and the batch is acidified with acetic acid. The product which precipitates is filtered off and dried in an oven.
Yield: 129 parts=93%, melting point 176.degree. C.
EXAMPLE 3
4-Phenyl-thiazolylmalodinitrile
The procedure followed is as described in Example 1, except that instead of triethylamine 43 parts of piperidine are employed.
Yield: 112 g.
EXAMPLE 4
4-Phenyl-thiazolylmalodinitrile
The procedure followed is as described in Example 1, except that instead of triethylamine 30 parts of 30% strength ammonia are employed.
Yield 68%.
EXAMPLE 5
4-Phenyl-thiazolylmalodinitrile
The procedure followed is as described in Example 1, except that instead of triethylamine 143 parts of sodium carbonate dissolved in a little water are added.
Yield: 91%.
EXAMPLE 6
4-Phenyl-thiazolylmalodinitrile
The procedure followed is as described in Example 1, but instead of alcohol 600 parts of toluene are used. The product is isolated by distilling off the solvent.
Yield: 46%.
EXAMPLE 7
4-Methylthiazolylmalodinitrile
33 parts of malodinitrile are introduced into 400 parts of methanol; 57 parts of thiocyanatoacetone are added, followed by 50 parts of triethylamine added whilst cooling. The reaction mixture is stirred for 4 hours at room temperature and is then introduced into water, the batch is acidified with formic acid and the product is filtered off.
Yield: 71 parts=88%.
EXAMPLE 8
Methyl 4-methylthiazolylcyanoacetate
50 parts of methyl cyanoacetate, 50 parts of triethylamine and 57 parts of thiacyanoatoacetone are reacted in 400 parts of methanol as described in Example 7.
Yield: 79 parts=70%; melting point 235.degree. C.
EXAMPLE 9
14.3 parts of 1-thiacyanato-diethyl ketone are reacted with 6.6 parts of malodinitrile as described in Example 1.
Yield: 12.4 parts; melting point 225.degree. C.
EXAMPLE 10
4-Ethoxycarbonylmethylthiazolylmalodinitrile
19 parts of ethyl .gamma.-thiocyanato-acetoacetate are reacted with 6.6 parts of malodinitrile as described in Example 1.
Yield: 21 parts.
EXAMPLE 11
Tetrahydrobenzthiazolylmalodinitrile
15.4 parts of 1-thiocyanatocyclohexanone are reacted with 6.6 parts of malodinitrile as described in Example 1.
Yield: 14.3 parts.
EXAMPLE 12
Methyl tetrahydrobenzthiazolyl-cyanoacetate
The procedure described in Example 11 is followed, but instead of malodinitrile 10 parts of methyl cyanoacetate are employed.
Yield: 16 parts.
Compounds 13 to 34 are prepared by methods similar to the instructions given in Example 1.
EXAMPLE 35
18 parts of phenacyl thiocyanate, 10 parts of triethylamine and 16 parts of N,N-dimethylbarbituric acid in 100 parts of propanol are refluxed for 2 hours. The mixture is then cooled and the product filtered off. 10 parts of the compound of the formula ##STR35## are obtained.
Compounds 36 to 38 are prepared similarly.
Claims
I claim:
1. A process for the preparation of a thiazole derivative of the general formula ##STR39## where R.sup.1 and R.sup.2 are cyano; formyl; nitro; C.sub.1 -C.sub.8 alkanoyl, which is unsubstituted or substituted by chlorine, bromine or C.sub.1 -C.sub.4 -alkoxy; benzoyl which is unsubstituted or substituted by chlorine, bromine, methyl, ethyl, methoxy, ethoxy or cyano; naphthoyl; carboxylic acid ester groups derived from C.sub.1 -C.sub.8 -alkanols, C.sub.2 - to C.sub.8 -glycols, C.sub.2 -C.sub.8 -glycol ethers or phenols; carbamyl or sulfamoyl which is unsubstituted or substituted by C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxyalkyl, cyclohexyl or phenyl; C.sub.1 -C.sub.4 -alkylsulfonyl; C.sub.1 -C.sub.8 -alkylsulfinyl; phenylsulfonyl or phenylsulfinyl; R.sup.1 and R.sup.2 may also together be a cyclic radical selected from the group consisting of ##STR40## where aryl is phenyl which is unsubstituted or substituted by chlorine, bromine, methyl, ethyl, methoxy or ethoxy; and R.sup.2 may also be O.sub.2 N--C.sub.6 H.sub.4, NC--C.sub.6 H.sub.4, CH.sub.3 COC.sub.6 H.sub.4, ##STR41## R.sup.3 and R.sup.4 are hydrogen, CH.sub.3, C.sub.2 H.sub.5, C.sub.3 H.sub.7, C.sub.4 H.sub.9, C.sub.5 H.sub.11, C.sub.6 H.sub.5, C.sub.6 H.sub.13, C.sub.7 H.sub.15, C.sub.1 -bis C.sub.4 -alkyl-OC.sub.6 H.sub.4, (C.sub.1 -C.sub.4 -alkyl).sub.2 OC.sub.6 H.sub.3, Cl-C.sub.6 H.sub.4 CL.sub.2 C.sub.6 H.sub.3, BrC.sub.6 H.sub.4, Br.sub.2 C.sub.6 H.sub.3, C.sub.1 -C.sub.4 -alkyl-S-C.sub.6 H.sub.4, H.sub.5 C.sub.6 S-C.sub.6 H.sub.4, C.sub.1 -C.sub.4 -alkyl-CONHC.sub.6 H.sub.4, COOCH.sub.3, COOC.sub.2 H.sub.5, COOC.sub.3 H.sub.7, COOC.sub.4 H.sub.9, COC.sub.6 H.sub.5, COCH.sub.3 or CH.sub.2 -COO-C.sub.1 -C.sub.4 -alkyl; and R.sup.3 and R.sup.4 may also together be a cyclic radical selected from the group consisting of ##STR42## wherein a compound of the formula II ##STR43## is reacted with a compound of the formula III ##STR44## in the presence of a base selected from the group consisting of alkali metal compounds, alkaline earth metal compounds and amines.
2. The process as claimed in claim 1, wherein R.sup.1 and R.sup.2 are CN, CHO, NO.sub.2, COCH.sub.3, COC.sub.2 H.sub.5, COC.sub.3 H.sub.7, COCH.sub.2 CL, COCHCl.sub.2, COC.sub.6 H.sub.5, COC.sub.6 H.sub.4 Cl, COOCH.sub.3, COOC.sub.2 H.sub.5, COOC.sub.3 H.sub.7, COOC.sub.4 H.sub.9, COOC.sub.6 H.sub.5, COO(CH.sub.2).sub.3 OCH.sub.3, COO(CH.sub.2).sub.3 OC.sub.2 H.sub.5, CONHCH.sub.3, CONHC.sub.2 H.sub.5, CONHC.sub.3 H.sub.7, CONHC.sub.4 H.sub.9, CON(CH.sub.3).sub.2, CON(C.sub.2 H.sub.5).sub.2, CONH.sub.2, CONHC.sub.6 H.sub.5, ##STR45##
3. The process as claimed in claim 1, wherein said base is selected from the group consisting of NaOH, KOH, Ca(OH).sub.2, Ba(OH).sub.2, Mg(OH).sub.2, Na.sub.2 CO.sub.3, K.sub.2 CO.sub.3, Li.sub.2 CO.sub.3, NaOCH.sub.3, NaOC.sub.2 H.sub.5, KOC(CH.sub.3).sub.3, KOCH.sub.3, NH.sub.3, ethylamine, piperidine, pyrrolidine, N(CH.sub.3).sub.3, N(C.sub.2 H.sub.5).sub.3, N(C.sub.4 H.sub.9).sub.3, N(CH.sub.2 CH.sub.2 OH).sub.3, C.sub.6 H.sub.5 N(CH.sub.3).sub.2 and pyridine.
4. The process as claimed in claim 1, wherein a compound of the formula ##STR46## where B.sup.1 and B.sup.2 are cyano; C.sub.1 -C.sub.4 -alkoxy-carbonyl; C.sub.1 -C.sub.4 -alkanoyl; or carbamoyl substituted by C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxyalkyl, cyclohexyl or phenyl; and B.sup.3 and B.sup.4 are unsubstituted or chlorine-, bromine-, C.sub.1-4 -alkoxy-, methyl-, acetylamino- or C.sub.1 -C.sub.4 -alkylmercapto-substituted phenyl, methyl or ethyl, is prepared.
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| US3498997 | 1970-03-01 | Laliberte | |
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| BEX477772 | 1948-12-01 | ||
| DEX1913472 | 1969-11-01 | ||
| GBX609919 | 1948-10-01 | ||
| GBX1192701 | 1970-05-01 |
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