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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354023Generated: October 25, 2026

Water → [1,1'-Biphenyl]-4-yl-(5,11-dihydro-10H-dibenzo[b,e][1,4]diazepin-10-yl)methanone

https://huagongshe.com/reaction/1354023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
Reactant10,11-Dihydro-5h-dibenzo[b,e][1,4]diazepineHCID 36046—
Reactant4-Phenylbenzoyl chlorideHCID 84151—
SolventDimethylformamideHCID 6228—
Product[1,1'-Biphenyl]-4-yl-(5,11-dihydro-10H-dibenzo[b,e][1,4]diazepin-10-yl)methanoneHCID 982104038.3%

Reaction Steps

4-Biphenyl-carbonyl chloride (1.19 g) dissolved in N,N-dimethylformamide (10 mL) was added dropwise to an ice cooled solution of 5,11-dihydro-10H-dibenzo[b,e][1,4]diazepine (0.98 g) in N,N-dimethylformamide (10 mL). After stirring at room temperature overnight, the reaction mixture was poured into water and dichloromethane. The organic layer was sequentially washed with water and saturated sodium bicarbonate, and dried over anhydrous sodium sulfate. The solution was filtered through a short column of Magnesol® and eluted with additional dichloromethane. The combined eluate was refluxed with gradual addition of hexane until incipient crystallization occurred. Cooling and filtration provided the title compound (0.72 g), m.p. 180–182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223752B2
Source datasetuspto-grants-2007_05
ORD IDord-99cf32bbe09149de9fdbdaddf6d43e28
Source noteuspto-grants-2007_05