Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635820Generated: November 1, 2026

Diisopropylethylamine → HCID 9865339, compound

https://huagongshe.com/reaction/1635820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-4-(trifluoromethyl)pyrimidine-5-carbonyl chlorideHCID 2736708—
Reactant10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepineHCID 15547048—
SolventDichloromethaneHCID 6344—
ProductHCID 9865339HCID 986533982.1%

Reaction Steps

2-Chloro-4-(trifluoromethyl)pyrimidine-5-carbonyl chloride (2.57 g) was added gradually to an ice-cooled solution of 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]-benzodiazepine, (1.84 g) and diisopropylethylamine (1.37 g) in dichloromethane (50 ml). After stirring at room temperature for 18 hours, the reaction mixture was washed with water and saturated aqueous sodium bicarbonate. The dichloromethane solution was dried over anhydrous sodium sulfate and filtered through a short column of hydrous sodium magnesium silicate and further eluted with several volumes of dichloromethane. The combined organic phase was concentrated on a hot plate with the gradual addition of hexane until crystallization occurred. After cooling, the crystals were collected by filtration to yield the title compound (3.22 g), m.p. 221-223° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511974B1
Source datasetuspto-grants-2003_01
ORD IDord-40ead30b06c24697b240b840c20fbe88
Source noteuspto-grants-2003_01