Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium Chloride → N-(2-Pyridinylmethyl)-N-(methylsulfonyl)-4-(tetradecyloxy)benzamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | N-(pyridin-2-ylmethyl)methanesulfonamide | HCID 4657001 | — |
| 반응물 | Benzoyl chloride, 4-(tetradecyloxy)- | HCID 9998158 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-(2-Pyridinylmethyl)-N-(methylsulfonyl)-4-(tetradecyloxy)benzamide | HCID 19014924 | 90.3% |
반응 단계
To a room temperature solution of 0.428 g of washed 50% sodium hydride in 15 ml of dry tetrahydrofuran is added, via cannula, 1.58 g of product from Example 121 dissolved in 20 ml of dry tetrahydrofuran. The mixture is stirred for 2 hours and 3.0 g of product from Example 3 dissolved in 20 ml of dry tetrahydrofuran is added, via cannula. After stirring at room temperature for 30 minutes, the reaction is heated at reflux temperature for 2 hours. The cooled mixture is poured into half saturated sodium chloride and extracted with chloroform. The organic layer is dried and concentrated in vacuo. The residue is purified by chromatography (silica gel: 15-40% ethyl acetate/hexane) to give 3.85 g of the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05208247 |
| 출처 데이터셋 | uspto-grants-1993_05 |
| ORD ID | ord-d1044c7f8f5c471bb0204eee3a29fb07 |
| 출처 메모 | uspto-grants-1993_05 |