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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978172Generated: October 29, 2026

Potassium Carbonate → (2-Chloro-4-fluorophenyl)-(6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-methanone

https://huagongshe.com/reaction/1978172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-fluorobenzoyl chlorideHCID 2736546—
Reactant6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepineHCID 11030760—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(2-Chloro-4-fluorophenyl)-(6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-methanoneHCID 1589593062%

Reaction Steps

To a solution of 6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepine of Step B (12.8 g, 65 mmol) in dimethylformamide (120 mL) under nitrogen was added potassium carbonate (19.76 g, 143 mmol). The mixture was cooled and treated dropwise with a solution of crude 2-chloro-4-fluorobenzoyl chloride of Step C (78 mmol) in dimethylformamide (50 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. The crude material was purified by flash chromatography (on silica Merck-60, hexane-ethyl acetate gradient from 95:5 to 80:20) to provide the pure title compound (14.25 g) along with some less pure material (2.7 g). The pure material is an off-white crystalline solid, which is used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235900B1
Source datasetuspto-grants-2001_05
ORD IDord-d4fec63d02104986a0266bde531f8902
Source noteuspto-grants-2001_05