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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230540생성일: 2026년 10월 25일

2-Methoxyaniline → N-(2-methoxyphenyl)4-(4-methyl-1-piperazinyl)-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/230540

반응식

참여 물질

역할이름HCID투입량
반응물2-MethoxyanilineHCID 7000—
반응물Benzenesulfonyl chloride, 4-chloro-3-nitro-HCID 7323—
반응물1-MethylpiperazineHCID 53167—
반응물4-chloro-N-(2-methoxyphenyl)-3-nitrobenzenesulfonamideHCID 2887683—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물N-(2-methoxyphenyl)4-(4-methyl-1-piperazinyl)-3-nitrobenzenesulfonamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566715B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-679f2da9fb2340dfa968b7e0ae2164cf
출처 메모uspto-grants-2009_07