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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248713생성일: 2026년 10월 25일

Triethylamine → 2-[2-[N-(4-Fluoro-3-trifluoromethylphenyl)sulfamoyl]-acetylamino]acetic Acid Ethyl Ester

https://huagongshe.com/reaction/248713

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Glycine ethyl ester, hydrochlorideHCID 2723640—
반응물2-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl]acetic acidHCID 19764008—
반응물HCID 178526939HCID 178526939—
용매DimethylformamideHCID 6228—
생성물2-[2-[N-(4-Fluoro-3-trifluoromethylphenyl)sulfamoyl]-acetylamino]acetic Acid Ethyl EsterHCID 15676557—

반응 조건

온도-10 °C

반응 단계

Under nitrogen, 1.81 g (6 mmol) of 2-[2-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl]acetic acid, 0.845 g (6 mmol) of glycine ethyl ester hydrochloride (98%), and 0.919 g (6 mmol) of hydroxybenzotriazole, hydrate, are added to 100 ml of dimethylformamide and the mixture is cooled to -10° C. under agitation. Then 0.607 g (6 mmol) of triethylamine is added thereto, the mixture is agitated for 10 minutes and combined with 1.24 g (6 mmol) of dicyclohexylcarbodiimide. The mixture is stirred for another hour at the low temperature and then overnight without cooling. The mixture is suctioned off from the solid matter, the solution is concentrated to dryness under vacuum, and the residue is distributed between sodium bicarbonate solution and ethyl acetate. The ethyl acetate solution is washed with water, dried over sodium sulfate, and concentrated to dryness under vacuum. The residue is crystallized from ethyl acetate/hexane, thus obtaining 1.72 g (74.1% of theory) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210290
출처 데이터셋uspto-grants-1993_05
ORD IDord-8aa71a47b68641a79a3ac204511d370e
출처 메모uspto-grants-1993_05