Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Methoxyaniline → N-(2-methoxyphenyl)4-(4-methyl-1-piperazinyl)-3-nitrobenzenesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Methoxyaniline | HCID 7000 | — |
| 반응물 | Benzenesulfonyl chloride, 4-chloro-3-nitro- | HCID 7323 | — |
| 반응물 | 1-Methylpiperazine | HCID 53167 | — |
| 반응물 | 4-chloro-N-(2-methoxyphenyl)-3-nitrobenzenesulfonamide | HCID 2887683 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(2-methoxyphenyl)4-(4-methyl-1-piperazinyl)-3-nitrobenzenesulfonamide | HCID 22272549 | — |
반응 단계
The compound was prepared from 4-chloro-3-nitrobenzenesulfonylchloride (1 g, 3.9 mmol), 2-methoxyaniline (0.53 mL, 4.7 mmol) and pyridine (1.6 mL) in CH2Cl2 (2 mL). 4-Chloro-N-(2-methoxyphenyl)-3-nitrobenzenesulfonamide (0.345 mg) was reacted with N-methylpiperazine (0.144 mL) to afford N-(2-methoxyphenyl)-4-(4-methyl-1-piperazinyl)-3-nitrobenzenesulfonamide which was treated with Raney-Ni and hydrazine monohydrate. The final product was isolated as its HCl salt 1H NMR (DMSO-d6) δ 7.185 (dd, 1H), 7.08 (dt, 1H), 6.975 (d, 1H), 6.91-6.94 (m, 2H); 6.84 (dt, 1H), 3.56 (s, 3H), 3.42-3.47 (m, 2H), 3.22-3.24 (m, 2H), 2.95 (bt, 2H), 2.79 (bs, 3H); MS (posESI) m/z=376.2 (M+H+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07566715B2 |
| 출처 데이터셋 | uspto-grants-2009_07 |
| ORD ID | ord-679f2da9fb2340dfa968b7e0ae2164cf |
| 출처 메모 | uspto-grants-2009_07 |