참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 8-Amino-5,6,7,8-tetrahydroquinoline | HCID 11355564 | — |
| 반응물 | 8-Hydroxy-4-methoxy-5,6,7,8-tetrahydroquinoline | HCID 22018824 | — |
| 생성물 | 4-Methoxy-5,6,7,8-tetrahydroquinolin-8-amine | HCID 22018617 | 68% |
반응 단계
8-amino-4-methoxy-5,6,7,8-tetrahydroquinoline was prepared in 68% yield from 8-hydroxy-4-methoxy-5,6,7,8-tetrahydroquinoline (preparation and characterization described by: Uchida, M.; Morita, S.; Chihiro, M.; Kanbe, T.; Yamasaki, K.; Yabuuchi, Y.; Nakagawa, K. Chem. Pharm. Bull. 1989, 37, 1517-1523.) using the same procedure employed to prepare 8-amino-5,6,7,8-tetrahydroquinoline (according to the procedures described in Bridger et al. U.S. patent application U.S. Ser. No. 09/535,314). 1H NMR (CDCl3) δ 1.59-2.15 (m, 6H), 2.60-2.65 (m, 2H), 3.84 (s, 3H), 3.95 (dd, 1H, J=6.0, 9.0 Hz), 6.61 (d, 1H, J=6.0 Hz). 8.32 (d, 1H, J=6.0 Hz); 13C NMR (CDCl3) δ 19.53, 22.89, 31.94, 51.57, 55.62, 104.04, 120.94, 148.52, 160.42, 163.71; ES-MS m/z 179 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07354934B2 |
|---|
| 출처 데이터셋 | uspto-grants-2008_04 |
|---|
| ORD ID | ord-e5715f3d331e440da824dbe3f4ccced7 |
|---|
| 출처 메모 | uspto-grants-2008_04 |
|---|