Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478373Generated: October 31, 2026

Ammonium Chloride → HCID 178519406, compound

https://huagongshe.com/reaction/478373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantHCID 18001036HCID 18001036—
SolventDimethylformamideHCID 6228—
ProductHCID 178519406HCID 17851940681.3%

Reaction Conditions

Temperature115 °C

Reaction Steps

5-Cyanomethyl-1-(4-phenyl-2-chlorobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine (1 g), ammonium chloride (0.4 g) and sodium azide (0.48 g) are suspended in dimethylformamide (10 ml), and the mixture is heated at 110-120° C. for 16 hours. To the mixture are added ammonium chloride (0.4 g) and sodium azide (0.48 g), and the mixture is heated for 16 hours. The mixture is evaporated to remove dimethylformamide, and the resultant is acidified with a 1N hydrochloric acid. The mixture is extracted with chloroform, and the organic layer is washed with water, dried over magnesium sulfate, and concentrated. The residue is purified by silica gel column chromatography (solvent; dichloromethane→dichloromethane:methanol=20:1), and the resulting oily product is crystallized from diethyl ether to give 5-(5-tetrazolyl)methyl-1-(4-phenyl-2-chlorobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine (0.9 g) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642223B2
Source datasetuspto-grants-2003_11
ORD IDord-672413e56fe84aeead12004cb08c00ff
Source noteuspto-grants-2003_11