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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457701Generated: October 30, 2026

Water → N-[4-[(6,11-Dihydro-5H-dibenz[b,e]azepin-5-yl)carbonyl]-phenyl][1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/reaction/1457701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6,11-Dihydro-5H-dibenz[b,e]azepineHCID 67974—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(2-Phenylbenzoylamino)-benzoylchlorideHCID 11450501—
SolventDichloromethaneHCID 6344—
SolventEthyl acetate hexaneHCID 21226206—
ProductN-[4-[(6,11-Dihydro-5H-dibenz[b,e]azepin-5-yl)carbonyl]-phenyl][1,1'-biphenyl]-2-carboxamideHCID 2209994733.4%

Reaction Steps

A mixture of 6,11-dihydro-5H-dibenz[b,e]azepine (0.195 g), 4-[([1,1'-biphenyl]-2-carbonyl)amino]benzoyl chloride (0.41 g) and 0.155 g of N,N-diisopropylethylamine in 12 ml of dichloromethane is stirred at room temperature for 3 hours. The mixture is poured into water and extracted with dichloromethane. The extract is washed with H2O, saturated NaHCO3, H2O, brine and dried (Na2SO4). The solution is filtered through a thin pad of hydrous magnesium silicate and the filter pad washed with dichloromethane. The filtrate is concentrated to dryness to give 0.66 g of a yellow l , solid. Chromatography on thick layer silica gel plates with hexane-ethyl acetate (1.5:1) gives crystals (0.165 g) (from dichloromethane-ethyl acetate), m.p. 224° C.-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849735
Source datasetuspto-grants-1998_12
ORD IDord-28c6b7f885f443c58fb52e2651d50465
Source noteuspto-grants-1998_12