Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-(3-Chloro-2-cyanophenoxy)benzenesulfonyl chloride → 4-(3-chloro-2-cyano-phenoxy)-N-[3-(2-dimethylamino-ethoxy)-4-trifluoromethyl-phenyl]-benzenesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-(3-Chloro-2-cyanophenoxy)benzenesulfonyl chloride | HCID 2776917 | — |
| 반응물 | Benzenamine, 3-[2-(dimethylamino)ethoxy]-4-(trifluoromethyl)- | HCID 17756283 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 4-(3-chloro-2-cyano-phenoxy)-N-[3-(2-dimethylamino-ethoxy)-4-trifluoromethyl-phenyl]-benzenesulfonamide | HCID 10165761 | — |
반응 단계
To a mixture of 3-(2-dimethylamino-ethoxy)-4-trifluoromethyl-phenylamine (0.10 g, 0.4 mmol) in CHCl3 (2.5 mL) was added 4-(3-chloro-2-cyano-phenoxy) benzenesulfonyl chloride (0.13 g, 0.4 mmol) at rt. After stirring at rt for 72 h, the solvent was evaporated and the residue was purified by vacuum filtration through silica gel eluting successively with 4% MeOH in CH2Cl2 and 10% MeOH in CH2Cl2 followed by a mixture of CH2Cl2, MeOH and conc. NH4OH (90:10:1). The solvent was removed from the desired fractions and the residue was recrystallized from a mixture of MeOH and EtOAc to afford the title compound as a white solid; yield 0.01 g (5%): LCMS 540 (M++H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06849635B2 |
| 출처 데이터셋 | uspto-grants-2005_02 |
| ORD ID | ord-f654829ee46b47468eb0b6f8ed977fb2 |
| 출처 메모 | uspto-grants-2005_02 |