돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1517073생성일: 2026년 10월 25일

4-(1-Pyrrolidinyl)piperidine → [6-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridin-2-yl]-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanone

https://huagongshe.com/reaction/1517073

반응식

참여 물질

역할이름HCID투입량
반응물4-(1-Pyrrolidinyl)piperidineHCID 78703—
반응물3-Methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acidHCID 57441124—
반응물6-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acid methyl esterHCID 57441125—
반응물6-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acidHCID 86637420—
생성물[6-Chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridin-2-yl]-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanoneHCID 44547211—

반응 단계

In analogy to the procedure described for example 1, 6-chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acid [prepared from 6-chloro-3-methyl-5-(3-trifluoromethyl-phenyl)-pyridine-2-carboxylic acid methyl ester (intermediate 2) by saponification in analogy to the procedure described for intermediate 1B] was reacted with 4-pyrrolidin-1-yl-piperidine to give the title compound as light brown solid. MS: 452.1 (MH+, 1Cl).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08227613B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-62cfcf0d424047f9a85b9bde9e2565c1
출처 메모uspto-grants-2012_07