Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
m-Anisoyl chloride → 2-(3-Methoxybenzoylamino)-4-methylthiazole-5-carboxylic Acid Benzylamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | m-Anisoyl chloride | HCID 74374 | — |
| 반응물 | N-Benzyl-2-imino-4-methyl-2,3-dihydro-1,3-thiazole-5-carboximidic acid | HCID 210824 | — |
| 생성물 | 2-(3-Methoxybenzoylamino)-4-methylthiazole-5-carboxylic Acid Benzylamide | HCID 3713816 | 34% |
반응 단계
Following the procedure as described in Example 2, making variations only as required to use 3-methoxybenzoyl chloride in place of benzoyl chloride to react with 2-amino-4-methylthiazole-5-carboxylic acid benzylamide, the title compound was obtained as a white solid in 34% yield; m.p. 75-77° C.; 1H NMR (CDCl3, 300 MHz) δ 7.43-7.31 (m, 8H), 7.12 (td, J=2.4, 6.7 Hz, 1H), 5.97 (t, J=5.6 Hz, 1H), 4.58 (d, J=5.6 Hz, 2H), 3.82 (s, 3H), 2.47 (s, 3H); MS (ES+) m/z 382.1 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08541457B2 |
| 출처 데이터셋 | uspto-grants-2013_09 |
| ORD ID | ord-67e90ad412c9495b9d57483c574bfd58 |
| 출처 메모 | uspto-grants-2013_09 |