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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ethyl 4-amino-1-piperidinecarboxylate | HCID 100867 | — |
| 반응물 | 1-(4-Fluorobenzyl)-2-chlorobenzimidazole | HCID 3020241 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | Ethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-YL]amino]piperidine-1-carboxylate | HCID 3019916 | 40.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04835161 |
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| 출처 데이터셋 | uspto-grants-1989_05 |
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| ORD ID | ord-4cf92ec6199f4e86980cc57881e512a1 |
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| 출처 메모 | uspto-grants-1989_05 |
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