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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2101975생성일: 2026년 10월 25일

Acetonitrile → 1-({5-[3,5-Bis(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}methyl)-2-propyl-4-(trifluoromethyl)-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/2101975

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Cesium carbonateHCID 10796—
반응물5-[3,5-Bis(trifluoromethyl)phenyl]-3-(chloromethyl)-1,2,4-oxadiazoleHCID 2780957—
반응물2-propyl-4-(trifluoromethyl)-1H-indole-5-carbonitrileHCID 67405155—
용매Ethyl AcetateHCID 8857—
생성물1-({5-[3,5-Bis(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}methyl)-2-propyl-4-(trifluoromethyl)-1H-indole-5-carbonitrileHCID 8662067381%

반응 조건

온도75 °C

반응 단계

A mixture of 2-propyl-4-(trifluoromethyl)-1H-indole-5-carbonitrile (0.040 g, 0.16 mmol), 5-[3,5-bis(trifluoromethyl)phenyl]-3-(chloromethyl)-1,2,4-oxadiazole (0.058 g, 0.17 mmol), Cs2CO3 (0.057 g, 0.17 mmol) and CH3CN (4 mL) was stirred at 75° C. for 1.5 h. The mixture was diluted with EtOAc (25 mL), washed with water (15 mL), and brine (15 mL). The organic portion was dried (MgSO4), filtered, and concentrated. The concentrated material was treated with 10% Et2O in hexanes (10 mL) and stirred for 2 h. The resulting solid was filtered, rinsed with hexanes, and dried to afford the title compound (0.070 g, 81%) as a light tan solid: 1H NMR (400 MHz, DMSO-d6) δ 8.53 (s, 2H), 8.50 (s, 1H), 8.03 (d, J=8.6 Hz, 1H), 7.75 (d, J=8.6 Hz, 1H), 6.59 (s, 1H), 5.90 (s, 2H), 2.90 (t, J=7.5 Hz, 2H), 1.79-1.70 (m, 2H), 0.98 (t, J=7.4 Hz, 3H); MS m/z 547 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07572820B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-922bcfbb88d4458d81ac02962cd54abd
출처 메모uspto-grants-2009_08