Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1-Phenethylamine, (+)- → (7bR,11aS)-N-[(1R)-1-phenylethyl]-1,2,7b,8,9,10,11,11a-octahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indol-6-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1-Phenethylamine, (+)- | HCID 643189 | — |
| 반응물 | tert-butyl (7bR,11aS)-6-bromo-1,2,7b,10,11,11a-hexahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indole-9(8H)-carboxylate | HCID 86586435 | — |
| 생성물 | (7bR,11aS)-N-[(1R)-1-phenylethyl]-1,2,7b,8,9,10,11,11a-octahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indol-6-amine | HCID 60071849 | — |
반응 단계
Using (R)-(−)-α-methylbenzylamine and following the procedures described in EXAMPLE 168, tert-butyl (7bR,11aS)-6-bromo-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 7, Part A was converted into the title compound of EXAMPLE 170. 1H NMR(CDCl3) δ: 7.40-7.20 (m, 5H), 6.17 (d, 1H, J=2.2 Hz), 6.10 (d, 1H, J=2.2 Hz), 4.35 (q, 1H, J=6.6 Hz), 3.56 (ABq, 2H, JAB=15.7 Hz), 3.50-3.42 (m, 1H), 3.29-3.21 (m, 2H), 3.15-2.80 (m, 5H), 2.58-2.48 (m, 1H), 2.00-1.85 (m, 2H), 1.45 (d, 3H, J=6.6 Hz). LRMS (ES)+: 366.4 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06699852B2 |
| 출처 데이터셋 | uspto-grants-2004_03 |
| ORD ID | ord-2ff45159dcb14379a40240fbc2fbf3a9 |
| 출처 메모 | uspto-grants-2004_03 |