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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 571848생성일: 2026년 10월 26일

Diisopropylethylamine → (R)-2-{2-Fluoro-4-[(2-trifluoromethyl-pyridine-4-carbonyl)-amino]-phenyl}-morpholine-4-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/571848

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-(Trifluoromethyl)pyridine-4-carboxylic acidHCID 14761447—
반응물(R)-tert-butyl 2-(4-amino-2-fluorophenyl)morpholine-4-carboxylateHCID 68325616—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물(R)-2-{2-Fluoro-4-[(2-trifluoromethyl-pyridine-4-carbonyl)-amino]-phenyl}-morpholine-4-carboxylic acid tert-butyl esterHCID 71086866—

반응 단계

Under N2, 2-(trifluoromethyl)-4-pyridinecarboxylic acid (CAS 131747-41-6) (64.4 mg, 337 μmol, Eq: 1.00) was dissolved in CH2Cl2 (1 ml). 1-chloro-N,N2-trimethypropenylamine (51.8 mg, 51.3 μl, 388 μmol, Eq: 1.15) was added dropwise. After 30 minutes at RT, a solution contained (R)-2-(4-Amino-2-fluoro-phenyl)-morpholine-4-carboxylic acid tert-butyl ester (100 mg, 337 μmol, Eq: 1.00) and ethyldiisopropylamine (109 mg, 140 μl, 842 μmol, Eq: 2.5) in DMF (1.00 ml) was added. The RM was stirred at RT over 1 hour. Control with TLC: the reaction was finished. The RM was extracted with EtOAc and 1M citric acid solution; the organic phase was dried over MgSO4; filtered; concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 10 g, 10% to 50% EtOAc in heptane) leading to 149 mg (82%) of a white foam. MS (EIC): 468.1 ([M−H]−)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029370B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-6cf179b61a7c43eaad51f11f8be1577c
출처 메모uspto-grants-2015_05