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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72347생성일: 2026년 10월 24일

Ammonium Acetate → N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamide

https://huagongshe.com/ko/reaction/72347

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium AcetateHCID 517165—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물N-(tert-Butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamideHCID 68288463—
용매MethanolHCID 887—
생성물N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamideHCID 68287917105.7%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828995B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e6e383aa11d742978b08a562cc141a0b
출처 메모uspto-grants-2014_09