Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1-(4-fluorophenyl)-N-methylmethanamine → 2-(6-{[2-(4-Methoxy-phenoxy)-ethyl]-methyl-amino}-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid 4-fluoro-benzylamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1-(4-fluorophenyl)-N-methylmethanamine | HCID 736860 | — |
| 반응물 | [2-(4-Methoxyphenoxy)ethyl](methyl)amine | HCID 2574637 | — |
| 반응물 | 2-(6-Iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid 4-fluoro benzylamide | HCID 86645558 | — |
| 생성물 | 2-(6-{[2-(4-Methoxy-phenoxy)-ethyl]-methyl-amino}-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid 4-fluoro-benzylamide | HCID 24955766 | 80% |
반응 단계
Following the procedure described in Example 14, making variations as required to replace 4-fluoro-N-methyl-benzylamine with [2-(4-methoxy-phenoxy)-ethyl]-methyl-amine to react with 2-(6-iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid 4-fluoro-benzylamide, the title compound was obtained in 80% yield. 1H NMR (400 MHz, CD2Cl2) δ 8.50 (s, 1H), 8.04 (s, 1H), 7.31-7.38 (m, 2H), 7.02-7.09 (m, 2H), 6.72-6.82 (m, 4H), 6.25 (bs, 1H), 4.55-4.59 (m, 2H), 4.18-4.23 (m, 2H), 4.01-4.08 (m, 2H), 3.69 (s, 3H), 3.31 (s, 3H), 2.71 (s, 3H); MS (ES+) m/z 508.2 (M+1), Rt=1.57 min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08314138B2 |
| 출처 데이터셋 | uspto-grants-2012_11 |
| ORD ID | ord-728c8be4cc764f9eb2c929c33cca2ec7 |
| 출처 메모 | uspto-grants-2012_11 |