• English
  • 简体中文
Login Register
Current Location: Home > Feedback Help Print

【结 构 式】

【分子编号】30750

【品名】methyl 3-[([2-[(diaminomethylene)amino]-1,3-thiazol-4-yl]methyl)sulfanyl]propanimidoate

【CA登记号】

【 分 子 式 】C9H15N5OS2

【 分 子 量 】273.3832

【元素组成】C 39.54% H 5.53% N 25.62% O 5.85% S 23.46%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(IX)

The reaction ot S-(2-aminothiazol-4-ylmethyl)isothiourea (I) with 3-chloropropionitrile (II) by means of NaOH in ethanol - water gives 3-(2-aminothiazol-4-ylmethylthio)propionitrile (III), which is condensed with benzoyl isothiocyanate (IV) in refluxing acetone to afford 3-[2-(3-benzoylthioureido)thiazol-4-ylmethylthio]propionitrile (V). The hydrolysis of (V) with K2CO3 in acetone - methanol - water yields 3-(2-thioureidothiazonl-4-ylmethylthio)propionitrile (VI), which by methylation with methyl iodide in refluxing ethanol is converted into 3-[2-(S-methylisothioureido)thiazol-4-ylmethylthio]propionitrile hydroiodide (VII). The reaction of (VII) with NH3 and NH4Cl in methanol at 90 C in a pressure vessel affords 3-(2-guanidinothiazol-4-ylmethylthio)propionitrile (VIII), which by partial alcoholysis with methanol by means of dry HCl in CHCl3 is converted into methyl 3-(2-guanidinothiazol-4-ylmethylthio)propionimidate (IX). Finally, this compound is treated with sulfamide in refluxing methanol.

1 Isomura, Y.; Ishii, Y.; Ito, N.; Takeda, M.; Yanagisawa, I.; Hirata, Y.; Tsukamoto, S. (Yamanouchi Pharmaceutical Co., Ltd.); Guanidinothiazole cpds., process for preparation and gastric inhibiting compsns. containing them. US 4283408 .
2 Hirata Y.; et al. (Yamanouchi Pharmaceutical Co., Ltd.); Novel amidine derivative and its preparation. BE 0882071; DE 2951675; DE 3008056; FR 2450827; GB 2052478; GB 2055800; JP 55118476; NL 7909321; NL 8001361 .
3 Blancafort, P.; Castaner, J.; Hillier, K.; Serradell, M.N.; Famotidine. Drugs Fut 1983, 8, 1, 14.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 30743 2-amino-4-([[amino(imino)methyl]sulfanyl]methyl)-1,3-thiazole C5H8N4S2 详情 详情
(II) 30744 3-chloropropanenitrile 542-76-7 C3H4ClN 详情 详情
(III) 30745 3-[[(2-amino-1,3-thiazol-4-yl)methyl]sulfanyl]propanenitrile 76823-89-7 C7H9N3S2 详情 详情
(IV) 23530 benzoyl isothiocyanate 532-55-8 C8H5NOS 详情 详情
(V) 30746 N-benzoyl-N'-(4-[[(2-cyanoethyl)sulfanyl]methyl]-1,3-thiazol-2-yl)thiourea C15H14N4OS3 详情 详情
(VI) 30747 N-(4-[[(2-cyanoethyl)sulfanyl]methyl]-1,3-thiazol-2-yl)thiourea C8H10N4S3 详情 详情
(VII) 30748 4-[[(2-cyanoethyl)sulfanyl]methyl]-2-[[imino(methylsulfanyl)methyl]amino]-1,3-thiazole C9H12N4S3 详情 详情
(VIII) 30749 N''-(4-[[(2-cyanoethyl)sulfanyl]methyl]-1,3-thiazol-2-yl)guanidine; 2-[4-(2-Cyanoethyl)methylthio]thioazolyl guanidine 76823-93-3 C8H11N5S2 详情 详情
(IX) 30750 methyl 3-[([2-[(diaminomethylene)amino]-1,3-thiazol-4-yl]methyl)sulfanyl]propanimidoate C9H15N5OS2 详情 详情
Extended Information