Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636374Generated: October 30, 2026

Dimethylformamide → HCID 21254872, compound

https://huagongshe.com/reaction/636374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-methylbenzoyl chlorideHCID 2737383—
Reactant6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepineHCID 11030760—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 21254872HCID 2125487255.8%

Reaction Steps

To a solution of 6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepine of Example 1, Step B (2.0 g, 10.1 mmol) in dimethylformamide (15 mL) under nitrogen was added potassium carbonate (4.1 g, 29.7 mmol). The mixture was treated dropwise with a solution of crude 5-fluoro-2-methyl benzoyl chloride of Step A (15.0 mmol) in dimethylformamide (10 mL). After stirring at room temperature for 15 minutes, the mixture was diluted with water and stirred to give a solid mass which was collected by filtration. The solid was dissolved in chloroform and washed with 1 N sodium hydroxide and brine. The organic layer was dried over sodium sulfate and evaporated to dryness to give a purple oil. The crude material was dissolved in dichloromethane and absorbed onto a silica Merck-60 flash column. Elution with 20% ethyl acetate in hexane provided 1.88 g (55.8%) of the title product as a foam which was crystallized by sonication from ethanol-hexane, m.p. 138-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194407B1
Source datasetuspto-grants-2001_02
ORD IDord-1d406af70ff54ca88b2ea8e573601466
Source noteuspto-grants-2001_02