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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2264562생성일: 2026년 10월 27일

Ammonia → 2,3-dihydro-5-(6-chloro-4-pyrimidinyloxy)-N-[4-(4-morpholinyl)-3-(trifluoromethyl)phenyl]-1H-indole-1-carboxamide

https://huagongshe.com/reaction/2264562

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물TriethylamineHCID 8471—
반응물TriphosgeneHCID 94429—
반응물4-Morpholino-3-(trifluoromethyl)anilineHCID 2771329—
반응물5-((6-Chloropyrimidin-4-yl)oxy)-1H-indoleHCID 57455156—
용매DichloromethaneHCID 6344—
생성물2,3-dihydro-5-(6-chloro-4-pyrimidinyloxy)-N-[4-(4-morpholinyl)-3-(trifluoromethyl)phenyl]-1H-indole-1-carboxamideHCID 86618290—

반응 단계

A solution containing 5-amino-2-(4-morpholinyl)benzotrifluoride (3.16 g, 12.8 mmol) and triethylamine (2.48 mL, 17.8 mmol) in CH2Cl2 (87 mL) is added dropwise to a stirred solution of bis(trichloromethyl)carbonate (1.26 g, 4.25 mmol) in CH2Cl2 (43 mL) at 0° C. After 30 min, a solution containing 5-[(6-chloro-4-pyrimidinyl)oxy]-1H-indole (Intermediate IVa; 3.48 g, 14 mmol) and triethylamine (1.96 mL, 14 mmol) in CH2Cl2 (52 mL) is added dropwise. After stirring for a further 15 min an aqueous solution of ammonia (100 mL of 2.5%) is added and the mixture is extracted with CH2Cl2. The combined extracts are washed with saturated aqueous NaCl, dried (K2CO3) and the solvent is evaporated off under reduced pressure to afford a crude product which is recrystallised from EtOH to give the title compound as a colourless crystalline solid: NMR (400 MHz; DMSO-d6) δ 2.11 (m, 4H), 3.20 (t, J=8.3 Hz, 2H), 3.68 (m, 4H), 4.16 (t, J=8.5 Hz, 2H), 6.96 (dd, J=8.6 Hz, J=2.5 Hz, 1H), 7.09 (d, J=1.5 Hz, 1H), 7.28 (s, 1H), 7.52 (d, J=8.6 Hz, 1H), 7.84 (dd, J=8.8 Hz, J=2.5 Hz, 1H), 7.88 (d, J=8.8 Hz, 1H), 7.92 (d, J=2.3 Hz, 1H), 8.62 (s, 1H) and 8.77 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07855215B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-b54b38ec739c438c85042e262559ab30
출처 메모uspto-grants-2010_12