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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2354513생성일: 2026년 10월 24일

4-Methylmorpholine → N-(1S,2S)-[2-(3-Cyanophenyl)-3-(4-methoxyphenyl)-1-methylpropyl]-2-(4-trifluoromethyl-2-pyridyloxy)-2-methylpropanamide

https://huagongshe.com/ko/reaction/2354513

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물3-((2S,3S)-3-amino-1-(4-chlorophenyl)butan-2-yl)benzonitrileHCID 11587296—
반응물2-Methyl-2-(4-trifluoromethyl-2-pyridyloxy)propionic AcidHCID 22270491—
용매DichloromethaneHCID 6344—
생성물N-(1S,2S)-[2-(3-Cyanophenyl)-3-(4-methoxyphenyl)-1-methylpropyl]-2-(4-trifluoromethyl-2-pyridyloxy)-2-methylpropanamideHCID 11785548—

반응 단계

To a solution of N-(1S, 2S)-[3-(4-chlorophenyl)-2-(3-cyanophenyl)-1-methylpropyl]amine (Reference Example 4, 0.60 g, 2.1 mol) and 2-(4-trifluoromethyl-2-pyridyloxy)-2-methylpropionic acid (Reference Example 13, 0.58 g, 2.4 mmol) in 10 mL of CH2Cl2 was added N-methylmorpholine (0.46 mL, 4.2 mmol) and tris(pyrrolindinyl)phosphonium hexafluorophosphate (1.6 g, 3.2 mmol). After stirring at room temperature overnight, the reaction mixture was loaded onto a silica gel column eluted with 30% EtOAc in hexane to give the title compound. 1H NMR (500 MHz, CD3OD): δ 8.19 (d, 1H), 7.48 (d, 1H), 7.38-7.35 (m, 2H), 7.31 (d, 1H), 7.18 (s, 1H), 7.11 (d, 1H), 7.03 (d, 2H), 6.67 (d, 2H), 4.23 (m, 1H), 3.01 (dd, 1H), 2.83 (m, 1H), 2.61 (dd, 1H), 1.76 (s, 3H), 1.72 (s, 3H), 0.79 (d, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07754188B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-38e08ebd253649279bd3959214c4b68e
출처 메모uspto-grants-2010_07