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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47582생성일: 2026년 10월 23일

3-Quinolinecarboxaldehyde → (7bR,11aS)-N-(3-quinolinylmethyl)-1,2,7b,8,9,10,11,11a-octahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indol-6-amine

https://huagongshe.com/ko/reaction/47582

반응식

참여 물질

역할이름HCID투입량
반응물3-QuinolinecarboxaldehydeHCID 83641—
반응물tert-butyl (7bR,11aS)-6-amino-1,2,7b,10,11,11a-hexahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indole-9(8H) carboxylateHCID 86586437—
생성물(7bR,11aS)-N-(3-quinolinylmethyl)-1,2,7b,8,9,10,11,11a-octahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indol-6-amineHCID 60071909—

반응 단계

Using 3-quinolinecarboxaldehyde and following the procedures described in EXAMPLE 126, tert-butyl (7bR,11aS)-6-amino-1,2,7b,10,11,11a-hexahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indole-9(8H)-carboxylate from EXAMPLE 33, Part B was converted into the title compound of EXAMPLE 164. LRMS (ES)+: 403.4 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699852B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-54cbc3c9aa1a4abb89a40d04e35c3eb8
출처 메모uspto-grants-2004_03