Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-(1,3-Oxazol-5-yl)benzenesulphonyl chloride → N-[4-Chloro-2-(2-methyl-pyridine-4-carbonyl)phenyl]-4-oxazol-5-yl-benzenesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-(1,3-Oxazol-5-yl)benzenesulphonyl chloride | HCID 2776415 | — |
| 반응물 | (2-Amino-5-chloro-phenyl)-(2-methyl-pyridin-4-yl)-methanone | HCID 22327293 | — |
| 생성물 | N-[4-Chloro-2-(2-methyl-pyridine-4-carbonyl)phenyl]-4-oxazol-5-yl-benzenesulfonamide | HCID 10321702 | — |
반응 단계
The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 123 mg of (2-Amino-5-chloro-phenyl)-(2-methyl-pyridin-4-yl)-methanone and 122 mg of 4-oxazol-5-yl-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 2.78 (s, 3H), 7.29 (d,1H, J=2.8 Hz), 7.45 (m, 2H), 7.48 (s,1H), 7.55 (dd,1H, J=9.2 Hz, 2.8 Hz)), 7.67 (m, 3H), 7.83 (d, 2H, J=8.4 Hz), 8.03 (s,1H), 8.81 (d, 1H, J=5.6 Hz), 10.10 (s, 1H). MS: m/z454.9 (M++1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07420055B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-c43d67a0d52e4ebf8b7993002a49b695 |
| 출처 메모 | uspto-grants-2008_09 |