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HRID 1762817作成日:2026年10月26日

Ethyl 4-amino-1-piperidinecarboxylate → Ethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-YL]amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1762817

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4-amino-1-piperidinecarboxylateHCID 100867—
反応物1-(4-Fluorobenzyl)-2-chlorobenzimidazoleHCID 3020241—
溶媒ChloroformHCID 6212—
生成物Ethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-YL]amino]piperidine-1-carboxylateHCID 301991640.5%

反応条件

温度120 °C

反応手順

A mixture of 9.8 parts of ethyl 4-amino-1-piperidinecarboxylate and 15 parts of 2-chloro-1-(4-fluorophenylmethyl)-1H-benzimidazole was heated to 120° C. The mixture was stirred at 120° C. during 43 hours. After cooling, 100 parts of trichloromethane were added and the whole was thouroughly stirred. The mixture was washed with water. The aqueous layer was separated and the organic mixture was filtered and evaporated. The collected solid material was dissolved in 100 parts of water and subsequently 100 parts of 20% sodium hydroxide solution were added. The precipitate was filtered and dried in vacuo at 50° C., yielding 12.1 parts (40.5%) of ethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinecarboxylate; mp. 181° C. (compound 21).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04835161
出典データセットuspto-grants-1989_05
ORD IDord-4cf92ec6199f4e86980cc57881e512a1
出典メモuspto-grants-1989_05