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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 455421생성일: 2026년 10월 24일

4-Chloro-3-hydroxybenzoic acid → (4-Chloro-3-hydroxy-phenyl)-(cis-2,3,4a,5,6,10b-hexahydro-1H-benzo[f]quinolin-4-yl)-methanone

https://huagongshe.com/ko/reaction/455421

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-3-hydroxybenzoic acidHCID 141872—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물(4aS,10bR)-1,2,3,4,4a,5,6,10b-Octahydrobenzo[f]quinolineHCID 12327022—
생성물(4-Chloro-3-hydroxy-phenyl)-(cis-2,3,4a,5,6,10b-hexahydro-1H-benzo[f]quinolin-4-yl)-methanoneHCID 8665412346%

반응 단계

The title compound is prepared from 4-chloro-3-hydroxy-benzoic acid and cis-1,2,3,4,4a,5,6,10b-octahydro-benzo[f]quinoline following a procedure analogous to that described in Example 1 [2-(7-aza-1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexa-fluorophosphate is used]. Yield: 46% of theory; LC (method 4): tR=1.99 min; Mass spectrum (ESI+): m/z=342/344 (Cl) [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497281B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-95c00a6a547146e79c4a01f299ae3a33
출처 메모uspto-grants-2013_07