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HRID 72369作成日:2026年10月25日

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

https://huagongshe.com/reaction/72369

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium AcetateHCID 517165—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物N-(tert-Butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamideHCID 68288463—
溶媒MethanolHCID 887—
生成物N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamideHCID 68287917—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828994B2
出典データセットuspto-grants-2014_09
ORD IDord-862b77b448334435a0c2e674fe13fedc
出典メモuspto-grants-2014_09