돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248668생성일: 2026년 10월 26일

Triethylamine → 3-[(2-Acetylthiomethyl-3-phenylpropionyl)amino]-5-methylbenzoic acid

https://huagongshe.com/reaction/248668

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Acetylthiomethyl-3-phenyl-propionyl chlorideHCID 10377734—
반응물3-Amino-5-methylbenzoic acidHCID 18405678—
용매TetrahydrofuranHCID 8028—
생성물3-[(2-Acetylthiomethyl-3-phenylpropionyl)amino]-5-methylbenzoic acidHCID 1567014951.8%

반응 단계

3-Amino-5-methylbenzoic acid (1.9 g) is dissolved in a 60% aqueous solution of tetrahydrofuran (30 ml) containing triethylamine (2.3 g), and to the mixture is added dropwise a solution of 2-acetylthiomethyl-3-phenyl-propionyl chloride (3.2 g) in tetrahydrofuran (20 ml) with stirring under ice cooling, and the mixture is stirred at room temperature for 2 hours. Tetrahydrofuran is distilled off under reduced pressure, and the residue is extracted with ethyl acetate (100 ml). The extract is washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and then ethyl acetate is distilled off under reduced pressure. The residue is dissolved in acetonitrile and purified by a medium pressure column chromatography with CHP-20P (eluant, water-acetonitrile). The fractions containing the desired compound are collected and concentrated into dryness under reduced pressure to give the title compound (2.4 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210266
출처 데이터셋uspto-grants-1993_05
ORD IDord-2bcdfcdab4524984be5bd1e9b06e5e26
출처 메모uspto-grants-1993_05