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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745062Generated: October 30, 2026

Diethylamine → HCID 19608225, compound

https://huagongshe.com/reaction/745062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantDiethyl cyanophosphonateHCID 76257—
ReactantHCID 19607810HCID 19607810—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 19608225HCID 1960822573%

Reaction Steps

1-[4-(3-Carboxypropionylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.5 g) is dissolved in dimethylformamide (1 ml) and thereto is added dropwise diethyl cyanophosphate (0.25 g) under ice-cooling. The mixture is stirred at room temperature for 30 minutes and then cooled again with ice. Thereto are added dropwise a solution of diethylamine (0.11 g) in dimethylformamide (1 ml) and triethylamine (0.34 g). The mixture is stirred at room temperature for 16 hours. The solvent is distilled off under reduced pressure and water is added to the resulting residue. The mixture is extracted with dichloromethane. The organic layer is washed successively with diluted hydrochloric acid, water, saturated sodium hydrogen carbonate solution, water and saturated saline solution, and dried over magnesium sulfate. The solvent is distilled off under reduced pressure and the resulting residue is purified by silica gel column chromatography (eluent; ethyl acetate), and recrystallized from n-hexane/ethyl acetate to give 1-[4-(3-diethylaminocarbonylpropionylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.42 g) as colorless scales, m.p. 165°-167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559230
Source datasetuspto-grants-1996_09
ORD IDord-afa6bdbc2b14465d8e23dd0d750ea1ed
Source noteuspto-grants-1996_09