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【结 构 式】

【分子编号】60235

【品名】1-(2-chloroacetyl)-2-pyrrolidinecarbonitrile

【CA登记号】

【 分 子 式 】C7H9ClN2O

【 分 子 量 】172.61404

【元素组成】C 48.71% H 5.26% Cl 20.54% N 16.23% O 9.27%

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)

The reaction of adamantan-1-amine (I) with HNO3 and H2SO4 gives 3-nitroadamantan-1-amine (II), which is hydrolyzed with KOH in hot water to yield 3-hydroxyadamantan-1-amine (III). On the other hand, the reaction of chloroacetyl chloride (IV) with L-prolinamide (V) by means of K2CO3 in THF gives 1-(chloroacetyl)-L-prolinamide (VI), which is treated with trifluoroacetic anhydride in THF to yield the corresponding nitrile (VII). Finally 3-hydroxyadamantan-1-amine (III) is condensed with the 1-(chloroacetyl)-L-prolinenitrile (VII) by means of K2CO3 in dichloromethane to afford the target adamantane derivative.

1 Villhauer, E.B. (Novartis AG); N-Substd. 2-cyanopyrrolidines. EP 1137635; JP 2002531547; US 6166063; WO 0034241 .
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) 60231 tricyclo[3.3.1.1~3,7~]dec-1-ylamine; tricyclo[3.3.1.1~3,7~]decan-1-amine C10H17N 详情 详情
(II) 60232 3-nitrotricyclo[3.3.1.1~3,7~]dec-1-ylamine; 3-nitrotricyclo[3.3.1.1~3,7~]decan-1-amine C10H16N2O2 详情 详情
(III) 60233 3-aminotricyclo[3.3.1.1~3,7~]decan-1-ol C10H17NO 详情 详情
(IV) 11296 2-Chloroacetyl chloride; Chloroacetic chloride 79-04-9 C2H2Cl2O 详情 详情
(V) 36137 (2S)-2-pyrrolidinecarboxamide;L-prolinamide 7531-52-4 C5H10N2O 详情 详情
(VI) 60234 1-(2-chloroacetyl)-2-pyrrolidinecarboxamide C7H11ClN2O2 详情 详情
(VII) 60235 1-(2-chloroacetyl)-2-pyrrolidinecarbonitrile C7H9ClN2O 详情 详情
Extended Information