Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride → 2-[[6-Fluoro-2-(3,4,5-trimethoxyphenyl)quinazolin-4-yl]carbonyl]-6-methoxy-1,2,3,4-tetrahydroisoquinoline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 2920335 | — |
| 반응물 | 6-Fluoro-2-(3,4,5-trimethoxyphenyl)quinazoline-4-carboxylic acid | HCID 90410307 | — |
| 생성물 | 2-[[6-Fluoro-2-(3,4,5-trimethoxyphenyl)quinazolin-4-yl]carbonyl]-6-methoxy-1,2,3,4-tetrahydroisoquinoline | HCID 86267786 | 53.8% |
반응 단계
Reaction of 6-fluoro-2-(3,4,5-trimethoxyphenyl)quinazoline-4-carboxylic acid with 6-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride gave compound 105 (53.8% yield). 1H NMR (300 MHz, DMSO-d6) δ 2.84 and 2.90 (2t, 2H), 3.60 and 4.06 (2t, 2H), 3.76-3.3.81 (m, 6H), 3.85 and 3.92 (2s, 6H), 4.55 and 4.98 (2s, 2H), 6.50-7.27 (m, 3H), 7.62-7.86 (m, 3H), 7.98-8.07 (m, 1H), 8.23-8.28 (m, 1H); MS (ESI) m/z 504 ([M+H]+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09193707B2 |
| 출처 데이터셋 | uspto-grants-2015_11 |
| ORD ID | ord-6287eb9b1eb14069ae2acda45dbef84a |
| 출처 메모 | uspto-grants-2015_11 |