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 | 105.7% |
반응 단계
A solution of N-(tert-butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamide (657 mg), ammonium acetate (1.85 g) and sodium cyanoborohydride (166 mg) was stirred in methanol (12 ml) at 60° C. for 17 hours. The reaction solution was concentrated by rotary evaporation and the residue was taken up in ethyl acetate (50 ml). Then it was washed with 0.5 N aqueous sodium hydroxide solution (50 ml) and with saturated sodium chloride solution (50 ml), and the organic phase was dried over MgSO4, filtered and concentrated under reduced pressure. This gave the product (697 mg) with a molecular weight of 274.3 g/mol (C12H19FN2O2S), MS (ESI): m/e=275 (M+H+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08828995B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-e6e383aa11d742978b08a562cc141a0b |
| 출처 메모 | uspto-grants-2014_09 |