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【结 构 式】

【分子编号】26909

【品名】1-cyclopentylhydrazine

【CA登记号】

【 分 子 式 】C5H12N2

【 分 子 量 】100.16376

【元素组成】C 59.96% H 12.08% N 27.97%

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)

Reaction of triethyl orthopropionate (I) with malononitrile (II) at reflux temperature provided (1-ethoxypropylidene)malononitrile (III). Cyclopentanone (IV) was condensed with tert-butyl carbazate (V) to afford the corresponding hydrazone (VI). Subsequent reduction with sodium cyanoborohydride, followed by acid deprotection furnished cyclopentylhydrazine (VII). Then, condensation of (VII) with malononitrile derivative (III) produced pyrazole (VIII). Partial hydrolysis of the cyano group of (VIII) using concentrated sulfuric acid gave carboxamide (IX).

1 Bacon, E.R.; Singh, B.; Lesher, G.Y.; Lesher, L.E. (Sanofi-Synthelabo); 6-Heterocyclyl pyrazolo[3,4-d]pyrimidin-4-ones and compsns. and method of use. US 5294612 .
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) 10395 1,1,1-Triethoxypropane; 1,1-Diethoxypropyl ethyl ether; Triethyl orthopropionate 115-80-0 C9H20O3 详情 详情
(II) 12061 Malononitrile 109-77-3 C3H2N2 详情 详情
(III) 26907 2-(1-ethoxypropylidene)malononitrile C8H10N2O 详情 详情
(IV) 15113 cyclopentanone 120-92-3 C5H8O 详情 详情
(V) 10893 tert-butyl 1-hydrazinecarboxylate; tert-butyl carbazate 870-46-2 C5H12N2O2 详情 详情
(VI) 26908 tert-butyl 2-cyclopentylidene-1-hydrazinecarboxylate C10H18N2O2 详情 详情
(VII) 26909 1-cyclopentylhydrazine C5H12N2 详情 详情
(VIII) 26910 5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carbonitrile C11H16N4 详情 详情
(IX) 26911 5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamide C11H18N4O 详情 详情
Extended Information