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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 717484생성일: 2026년 10월 24일

6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride → 2-[[6,7-Dimethoxy-2-(4-fluorophenyl)quinazolin-4-yl]carbonyl]-6-methoxy-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/ko/reaction/717484

반응식

참여 물질

역할이름HCID투입량
반응물6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 2920335—
반응물6,7-Dimethoxy-2-(4-fluorophenyl)quinazoline-4-carboxylic acidHCID 90410706—
생성물2-[[6,7-Dimethoxy-2-(4-fluorophenyl)quinazolin-4-yl]carbonyl]-6-methoxy-1,2,3,4-tetrahydroisoquinolineHCID 8626840719.2%

반응 단계

Reaction of 6,7-dimethoxy-2-(4-fluorophenyl)quinazoline-4-carboxylic acid with 6-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride gave compound 111 (19.2% yield). 1H NMR (400 MHz, DMSO-d6) δ 2.81 and 3.05 (2t, 2H), 3.48-4.06 (m, 11H), 4.41 and 4.93 (2s, 2H), 6.66-6.92 (m, 3H), 7.14-7.27 (m, 1H), 7.37-7.41 (m, 1H), 7.51 and 7.54 (2s, 1H), 7.59-7.63 (m, 1H), 8.15-8.20 (m, 1H), 8.31-8.35 (m, 1H); 19F (376 MHz, DMSO-d6) δ −113.0; MS (ESI) m/z 474 ([M+H]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09193707B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-f99f85c5174b485b8a4cedd0a14099c5
출처 메모uspto-grants-2015_11