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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 643149생성일: 2026년 10월 24일

Triethylamine → methyl (S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-4-[4-(6-hydroxy-2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidin-1-yl]-4-oxo-butanoate

https://huagongshe.com/ko/reaction/643149

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium BicarbonateHCID 516892—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물6-Hydroxy-3-piperidin-4-yl-3,4-dihydro-1H-quinazolin-2-oneHCID 21102207—
반응물1-methyl (S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-succinateHCID 86604295—
용매DimethylformamideHCID 6228—
생성물methyl (S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-4-[4-(6-hydroxy-2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidin-1-yl]-4-oxo-butanoateHCID 69071695—

반응 단계

A solution of 1.37 g (4.04 mmol) 1-methyl (S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-succinate, 1.42 g (4.40 mmol) TBTU, 0.63 mL (4.50 mmol) triethylamine and 1.00 g (4.04 mmol) 6-hydroxy-3-piperidin-4-yl-3,4-dihydro-1H-quinazolin-2-one in 10 mL DMF was stirred for 3 h at RT. The reaction mixture was poured onto 300 mL saturated NaHCO3 solution, the precipitated substance was suction filtered, washed with 50 mL water and dried at 60° C. in the circulating air dryer.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696209B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-42f657904f034372909ef82d7e496329
출처 메모uspto-grants-2010_04