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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2288677생성일: 2026년 10월 26일

Dimethylformamide → [2-Bromo-4-(3-methyl-pyrazol-1-yl)-phenyl]-(5,11-dihydro-benzo[b]pyrido[2,3-e][1,4]diazepin-6-yl)-methanone

https://huagongshe.com/reaction/2288677

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물2-Bromo-4-fluorobenzoyl chlorideHCID 2783346—
반응물6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepineHCID 11030760—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물[2-Bromo-4-(3-methyl-pyrazol-1-yl)-phenyl]-(5,11-dihydro-benzo[b]pyrido[2,3-e][1,4]diazepin-6-yl)-methanoneHCID 986885259.5%

반응 단계

To a solution of 6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepine of Example 1, Step B (5.15 g, 26.1 mmol) in dimethylformamide (70 mL) under nitrogen was added potassium carbonate (7.95 g, 57.51 mmol). The mixture was cooled and treated dropwise with a solution of crude 2-bromo-4-fluorobenzoyl chloride of Step A (31.37 mmol) in dimethylformamide (30 mL). After stirring at room temperature for 75 minutes the mixture was diluted with water and extracted with dichloromethane. The organic extracts were dried over magnesium sulfate and evaporated to dryness to give a brown solid foam. The crude material was dissolved in dichloromethane and absorbed onto a silica Merck-60 flash column. Elution with a hexane-ethyl acetate gradient (from 95:5 to 75:25) provided the pure title compound (6.18 g, 59.5%) along with some impure material (1.2 g). The pure material was triturated with hexane to provide an off-white solid foam, which was used as such in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06090803
출처 데이터셋uspto-grants-2000_07
ORD IDord-60a6c813a0504514b9bd07eeb63b73c2
출처 메모uspto-grants-2000_07