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【结 构 式】

【药物名称】SCRC-2941-18

【化学名称】4-(4-Chlorophenyl)-5-methylthiazol-2-amine

【CA登记号】82632-77-7

【 分 子 式 】C10H9ClN2S

【 分 子 量 】224.71363

【开发单位】Sagami (Originator)

【药理作用】Bone Diseases, Treatment of, IMMUNOMODULATING AGENTS, METABOLIC DRUGS, Treatment of Autoimmune Diseases, Treatment of Osteoporosis, Cytokine Production Inhibitors

合成路线1

Bromination of 4'-chloropropiophenone (I) afforded bromoketone (II). This was cyclized with thiourea (III) to produce the target 4-arylthiazole.

1 Hatanaka, Y.; Yamaguchi, K.; Kobori, T.; Tsuji, T.; Goda, K.; Yada, M.; 4-Phenylthiazole derivatives inhibit IL-6 secretion in osteoblastic cells and suppress bone weight loss in ovariectomized mice. Bioorg Med Chem Lett 1999, 9, 7, 957.
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) 29196 1-(4-Chlorophenyl)-1-propanone; 4-Chloropropiophenone 6285-05-8 C9H9ClO 详情 详情
(II) 29197 2-bromo-1-(4-chlorophenyl)-1-propanone C9H8BrClO 详情 详情
(III) 10180 Thiourea 62-56-6 CH4N2S 详情 详情
Extended Information