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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1762817생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1762817

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 4-amino-1-piperidinecarboxylateHCID 100867—
반응물1-(4-Fluorobenzyl)-2-chlorobenzimidazoleHCID 3020241—
용매ChloroformHCID 6212—
생성물Ethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-YL]amino]piperidine-1-carboxylateHCID 301991640.5%

반응 조건

온도120 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04835161
출처 데이터셋uspto-grants-1989_05
ORD IDord-4cf92ec6199f4e86980cc57881e512a1
출처 메모uspto-grants-1989_05