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【结 构 式】

【分子编号】35799

【品名】Spironolactone

【CA登记号】52-01-7

【 分 子 式 】C24H32O4S

【 分 子 量 】416.58168

【元素组成】C 69.2% H 7.74% O 15.36% S 7.7%

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:(VII)

Elimination of the thioacetyl group of spironolactone (VII) by treatment with NaOMe yielded canrenone (VIII). The title compound was then obtained by 1,6-conjugate addition of thiol (VI) to the dienone (VIII) in the presence of metallic sodium at 60 C.

1 Leblanc, G.; Noël, P.; Poirier, D.; Labrie, F.; Breton, E.; Luu-The, V.; Tremblay, M.R.; Spironolactone-related inhibitors of type II 17beta-hydroxysteroid dehydrogenase: Chemical synthesis, receptor binding affinities, and proliferative/antiproliferative activities. Bioorg Med Chem 1999, 7, 6, 1013.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(VI) 35798 4-[2-(1-piperidinyl)ethoxy]benzylhydrosulfide; [4-[2-(1-piperidinyl)ethoxy]phenyl]methanethiol C14H21NOS 详情 详情
(VII) 35799 Spironolactone 52-01-7 C24H32O4S 详情 详情
(VIII) 18027 3-Oxopregna-4,6-diene-21,17-carbolactone 976-71-6 C22H28O3 详情 详情
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