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【结 构 式】

【药物名称】Icoduline hydrochloride, CBS-113 A

【化学名称】2-(2-Hydroxy-4-methylphenylamino)thiazole hydrochloride

【CA登记号】110952-54-0, 138511-81-6 (free base)

【 分 子 式 】C10H11ClN2OS

【 分 子 量 】242.72897

【开发单位】Chauvin (Originator)

【药理作用】Antiinflammatory Ophthalmic Agents, Ocular Antiinflammatory and Antiinfective Agents, OCULAR MEDICATIONS, Ophthalmic Drugs

合成路线1

Condensation of benzoil isothiocyanate (I) with 6-amino-m-cresol in refluxing acetone gives N-benzoyl-N'-(2-hydroxy-4-methylphenyl)thiourea (II), which is hydrolyzed with sodium hydroxide to afford N-(2-hydroxy-4-methyl(phenyl)thiourea (III). Thiazolyl ring closure is obtained by addition of chloroacetaldehyde diethylacetal in refluxing ethanol catalyzed by p-toluenesulfonic acid. 2-(2-Hydroxy-4-methylphenyl)aminothiazole is then converted to its hydrochloride sait by bubbling gaseous hydrochloric acid.

1 Alazet, A.; Bonne, C.; Coquelet, C.; Sincholle, D. (Chauvin Laboratories SA); N-Substd. 2-amino-thiazoles, process for their pre. EP 0202157; ES 8900045; FR 2581063; JP 1987077375; US 4785008 .
2 Coquelet, C.; Bonne, C.; CBS-113 A. Drugs Fut 1987, 12, 6, 525.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
63311 2-chloro-1-ethoxyethyl ethyl ether; 2-chloro-1,1-diethoxyethane C6H13ClO2 详情 详情
(A) 23533 2-amino-5-methylphenol 2835-98-5 C7H9NO 详情 详情
(I) 23530 benzoyl isothiocyanate 532-55-8 C8H5NOS 详情 详情
(II) 23531 N-benzoyl-N'-(2-hydroxy-4-methylphenyl)thiourea C15H14N2O2S 详情 详情
(III) 23532 N-(2-hydroxy-4-methylphenyl)thiourea C8H10N2OS 详情 详情
Extended Information