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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288681Generated: November 2, 2026

Dimethylformamide → (5,11-Dihydro-pyrido[2,3-b][1,5]benzodiazepin-10-yl)-[2-fluoro-4-(3-methyl-pyrazol-1-yl)-phenyl]-methanone

https://huagongshe.com/reaction/2288681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Difluorobenzoyl chlorideHCID 588081—
Reactant6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepineHCID 11030760—
Product(5,11-Dihydro-pyrido[2,3-b][1,5]benzodiazepin-10-yl)-[2-fluoro-4-(3-methyl-pyrazol-1-yl)-phenyl]-methanoneHCID 2125488051%

Reaction Steps

To a solution of 6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepine of Example 1, Step B (3.0 g, 15.2 mmol) in dimethylformamide (35 mL) under nitrogen was added potassium carbonate (6.3 g, 45.6 mmol) followed by a solution of the crude 2,4difluorobenzoylchloride of Step A (22.8 mmol) in dimethylformamide (15 mL). After stirring at room temperature for 20 minutes, the reaction mixture was washed with water and stirred to give a solid which was collected by filtration. The solid was dissolved in chloroform and washed with 1 N sodium hydroxide and brine. The organic phase was dried over sodium sulfate and evaporated to dryness. The crude material was dissolved in dichloromethane and absorbed onto a silica Merck-60 flash column. Elution with 20% ethyl acetate in hexane provided the title compound (2.6 g, 51%) as a white foam which crystallized by sonication from hexane-ethanol, m.p. 161-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090803
Source datasetuspto-grants-2000_07
ORD IDord-fa1811c94b56499d93948998c8c32d5a
Source noteuspto-grants-2000_07