Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Acetylbenzenesulphonamide → 4-[3E-(2,4-Dimethoxy-5-pyridin-3-yl-phenyl)-acryloyl]-benzenesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Acetylbenzenesulphonamide | HCID 74065 | — |
| 반응물 | 2,4-Dimethoxy-5-pyridin-3-yl-benzaldehyde | HCID 21981113 | — |
| 생성물 | 4-[3E-(2,4-Dimethoxy-5-pyridin-3-yl-phenyl)-acryloyl]-benzenesulfonamide | HCID 10002459 | 51% |
반응 단계
The title compound was prepared by condensing 2,4-dimethoxy-5-pyridin-3-yl-benzaldehyde (Ex-104A) and 4-acetyl-benzenesulfonamide (Ex-26A) in a similar manner as described in Ex-22. Yellow solid, 51% yield, mp 253–255° C. 1H-NMR (DMSO-d6) δ 8.69 (d, J=1 Hz, 1H), 8.50 (d, J=4 Hz, 1H), 8.25 (d, J=9 Hz, 2H), 8.08 (d, J=15 Hz, 1H), 8.02 (s, 1H), 7.84–7.94 (m, 4H), 7.51 (s, 2H), 7.40–7.44 (m, 1H), 6.82 (s, 1H), 3.98 (s, 3H), 3.88 (s, 3H). MS m/z=424([M]+, 45%), 393 (100%). HMRS (EI) calcd. for C22H20N2O5S: 424.1093; found 424.1100.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07094801B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-ce21f1cc5c9b429bbe2772763daae429 |
| 출처 메모 | uspto-grants-2006_08 |