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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 512500생성일: 2026년 10월 26일

Ethanolamine → 1-(4-Cyano-benzyl)-6-methyl-4-oxo-5-(3-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid (2-hydroxy-ethyl)-amide

https://huagongshe.com/reaction/512500

반응식

참여 물질

역할이름HCID투입량
반응물EthanolamineHCID 700—
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물1-(4-Cyano-benzyl)-6-methyl-4-oxo-5-(3-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acidHCID 86711527—
용매DimethylformamideHCID 6228—
생성물1-(4-Cyano-benzyl)-6-methyl-4-oxo-5-(3-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid (2-hydroxy-ethyl)-amideHCID 73426831—

반응 단계

A solution of 1-(4-cyano-benzyl)-6-methyl-4-oxo-5-(3-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid (preparation 1, 70 mg, 0.102 mmol), TBTU (37 mg, 0.115 mmol), DIPEA (40 μL, 0.234 mmol) in DMF (0.5 mL) is stirred for 15 min at room temperature. Ethanolamine (7 μL, 0.116 mmol) is added and the reaction mixture is stirred for 1.5 h at room temperature. The reaction mixture is purified by preparative reversed-phase HPLC (Sunfire, gradient of methanol in water, 0.1% TFA, 60° C.). Yield: 16 mg (34% of theory); ESI mass spectrum: [M+H]+=456; Retention time HPLC: 1.34 min (Z002—005).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102624B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-10e8113607a843829feddaea839af203
출처 메모uspto-grants-2015_08