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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635853Generated: November 1, 2026

Diisopropylethylamine → HCID 10273764, compound

https://huagongshe.com/reaction/1635853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-[3-(trifluoromethyl)-1H-pyrazol-1-yl]benzoyl chlorideHCID 2780700—
Reactant10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepineHCID 15547048—
SolventDichloromethaneHCID 6344—
ProductHCID 10273764HCID 1027376484.3%

Reaction Steps

To a solution of 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]-benzodiazepine (0.88 g) and diisopropylethylamine (0.66 g) in dichloromethane (50 ml) was added the 4-(3-trifluoromethylpyrazol-1-yl)benzoyl chloride (1.40 g). 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 (1.70 g), m.p. 166-167° C.; MS, m/z: 423.3 (M+H)+, 845.4 (2M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511974B1
Source datasetuspto-grants-2003_01
ORD IDord-704277415c82455ab4a7b45c3aa2528a
Source noteuspto-grants-2003_01