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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264616생성일: 2026년 10월 26일

Triethylamine → {(2R,4S)-2-Benzyl-4-[(quinolin-4-ylmethyl)-amino]-piperidin-1-yl}-(3,5-bis-trifluoromethyl-phenyl)-methanone

https://huagongshe.com/reaction/264616

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3,5-Bis(trifluoromethyl)benzoic acidHCID 12889—
반응물Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
반응물(2R*,4S*)-2-Benzyl-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamineHCID 57202094—
용매DichloromethaneHCID 6344—
생성물{(2R,4S)-2-Benzyl-4-[(quinolin-4-ylmethyl)-amino]-piperidin-1-yl}-(3,5-bis-trifluoromethyl-phenyl)-methanoneHCID 10370818—

반응 단계

143 mg (561 mmol) of bis-(2-oxo-3-oxazolidinyl)phosphinic chloride and 144 μl (1.03 mmol) of triethylamine are added to a solution of 200 mg (467 mmol) of (2R*,4S*)-2-benzyl-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine and 113 mg (561 mmol) of 3,5-bis-(trifluoromethyl)-benzoic acid in 3 ml of methylene chloride, and the reaction mixture is left to stir at room temperature for 16 hours. It is then diluted with methylene chloride, and the organic phase is washed once each with 10% strength citric acid, 1N sodium bicarbonate solution and with brine, dried over magnesium sulfate and evaporated to dryness. The yellowish foam is chromatographed on silica gel with methylene chloride/methanol/conc. ammonia (1000:50:1). The title compound is obtained as yellow oil. TLC: methylene chloride/methanol/conc. ammonia (1000:50:1) Rf =0.34, FD-MS: M+ =667.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646144
출처 데이터셋uspto-grants-1997_07
ORD IDord-a28e90b29254441e88b48efc95beb591
출처 메모uspto-grants-1997_07