Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ammonium Acetate → N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ammonium Acetate | HCID 517165 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 반응물 | N-(tert-Butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamide | HCID 68288463 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamide | HCID 68287917 | — |
반응 단계
A solution of 0.66 g of N-(tert-butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamide, 1.85 g of ammonium acetate and 0.17 g of sodium cyanoborohydride in 12 ml of methanol was stirred at 60° C. for 17 hours. After the removal of the solvent under reduced pressure, the residue was taken up in 50 ml of ethyl acetate and washed twice with 30 ml of 0.5 N aqueous sodium hydroxide solution and 30 ml of saturated aqueous sodium chloride solution. The organic phase was dried over MgSO4 and concentrated by rotary evaporation. The crude product was subjected to a chiral separation.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08828994B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-862b77b448334435a0c2e674fe13fedc |
| 출처 메모 | uspto-grants-2014_09 |