Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Methoxyethylamine → 4-amino-N-(2-methoxyethyl)benzene-1-sulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Methoxyethylamine | HCID 8018 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Aminobenzenesulfonyl fluoride | HCID 66823 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 생성물 | 4-amino-N-(2-methoxyethyl)benzene-1-sulfonamide | HCID 16781918 | 65.4% |
반응 단계
A mixture of 2-methoxyethylamine (859 mg, 11.4 mmol), sulphanilyl fluoride (1.0 g, 5.71 mmol) and triethylamine (1.72 g, 22.9 mmol) in 1-butanol (15 ml) was heated at reflux for 18 hours. The mixture was allowed to cool and the volatiles were removed by evaporation. The residue was purified by chromatography eluting with ethyl acetate/hexane (50:50) increasing in polarity to (70:30) to give the title compound (860 mg, 65%). NMR: 2.78 (q, 2H), 3.15 (s, 3H), 3.25 (t, 2H), 5.87 (s, 2H), 6.58 (d, 2H), 7.10 (t, 1H), 7.40 (d, 2H); m/z 231.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06939872B2 |
| 출처 데이터셋 | uspto-grants-2005_09 |
| ORD ID | ord-d69b87f4c03c41eb9db78e5e4ada6c17 |
| 출처 메모 | uspto-grants-2005_09 |