Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-acetyl-N-(tert-butyldimethylsiloxy)benzenesulfonamide → 4-{3E-[2,4-Dimethoxy-5-(1-methyl-1H-indol-2-yl)phenyl]acryloyl}-N-(tert-butyldimethylsiloxy)benzenesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-acetyl-N-(tert-butyldimethylsiloxy)benzenesulfonamide | HCID 21082528 | — |
| 반응물 | 2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)benzaldehyde | HCID 21981006 | — |
| 용매 | Dichloromethane methanol | HCID 21226129 | — |
| 생성물 | 4-{3E-[2,4-Dimethoxy-5-(1-methyl-1H-indol-2-yl)phenyl]acryloyl}-N-(tert-butyldimethylsiloxy)benzenesulfonamide | HCID 11204233 | 19% |
반응 단계
The title compound was prepared in an analogous manner as Ex-1 using 4-acetyl-N-(tert-butyldimethylsiloxy)benzenesulfonamide (Ex-33A) and 2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)benzaldehyde (Ex-15A), 19% yield after preparative TLC (MeOH/CH2Cl2, 1:10), yellow solid, mp 129–131° C. 1H-NMR (300 MHz, CDCl3) δ 8.18 (d, J=15 Hz, 1H), 8.12 (d, J=8 Hz, 2H), 8.02 (d, J=8 Hz, 2H), 7.69 (s, 1H), 7.64 (d, J=8 Hz, 1H), 7.47 (d, J=15 Hz, 1H), 7.36 (d, J=7 Hz, 1H), 7.22–7.26 (m, 1H), 7.11–7.16 (m, 1H), 6.58 (s, 1H), 6.50–6.51 (m, 2H), 4.03 (s, 3H), 3.90 (s, 3H), 3.59 (s, 3H), 0.90 (s, 9H), 0.20 (s, 6H). HRMS (ESI) Calcd. for C32H39N2O6SSi: 607.2298 (M+H)+; Found: 607.2306.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07173129B2 |
| 출처 데이터셋 | uspto-grants-2007_02 |
| ORD ID | ord-a99088f3513544a4adc30804cfeadb12 |
| 출처 메모 | uspto-grants-2007_02 |