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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1978178생성일: 2026년 10월 25일

Potassium Carbonate → (6,11-Dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-(4-fluoro-2-trifluoromethyl-phenyl)-methanone

https://huagongshe.com/reaction/1978178

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-Fluoro-2-(trifluoromethyl)benzoyl chlorideHCID 605680—
반응물6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepineHCID 11030760—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물(6,11-Dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-(4-fluoro-2-trifluoromethyl-phenyl)-methanoneHCID 1551333033.1%

반응 단계

To a solution of 6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepine of Example 1, Step B (10.6 g, 53.8 mmol) in dimethylformamide (125 mL) under nitrogen was added potassium carbonate (22.4 g, 162 mmol). The mixture was cooled and treated dropwise with a solution of crude 2-trifluoromethyl-4-fluorobenzoyl chloride of Step A (81 mmol) in dimethylformamide (25 mL). After stirring at room temperature for 2 hours, the mixture was diluted with water and extracted with dichloromethane. The organic extracts were dried over magnesium sulfate and evaporated to dryness. The crude material was dissolved in dichloromethane and purified by flash chromatography (on silica Merck-60, hexane-ethyl acetate 80:20) to provide the pure title compound (6.9 g) which was crystallized by sonication from ethanol-hexane, m.p. 183-185° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06235900B1
출처 데이터셋uspto-grants-2001_05
ORD IDord-7c9f606b19ef4b62a9c436c6975e6e26
출처 메모uspto-grants-2001_05