Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Cesium carbonate → N-[3-[[2-(3,4-Dimethoxyphenyl)ethyl]methylamino]propyl]-N-(1-methylethyl)-3-(trifluoromethyl)benzenesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | N-Methylhomoveratrylamine | HCID 77039 | — |
| 반응물 | N-(3-chloropropyl)-N-(1-methylethyl)-3-trifluoromethylbenzenesulfonamide | HCID 23323132 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | N-[3-[[2-(3,4-Dimethoxyphenyl)ethyl]methylamino]propyl]-N-(1-methylethyl)-3-(trifluoromethyl)benzenesulfonamide | HCID 54053041 | — |
반응 단계
N-(3-chloropropyl)-N-(1-methylethyl)-3-trifluoromethylbenzenesulfonamide (23.4 g, 0.068 mol) and N-methylhomoveratrylamine (13.29 g, 0.068 mol) in xylene (250 mL) containing anhydrous potassium carbonate (4.68 g, 0.034 mol) and cesium carbonate (11.08 g, 0.034 mol) were heated and stirred for 21/2 days. The reaction was cooled, filtered and stripped to provide a gum with a small amount of crystalline material evident. Solution in diethyl ether, filtration of the small amount of solid and concentration of the filtrate provided the crude product (32.91 g). Chromatography first on dry column alumina then silica gel provided the same product as in the preceding example (11.84 g) as a gum.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04587360 |
| 출처 데이터셋 | uspto-grants-1986_05 |
| ORD ID | ord-a34e266674d745498b2980fb26cb4bec |
| 출처 메모 | uspto-grants-1986_05 |