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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603113Generated: October 28, 2026

Benzenesulfonyl chloride → HCID 10763869, compound

https://huagongshe.com/reaction/1603113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant(4-aminophenyl)-(2,3,4,5-tetrahydro-1-benzazepin-1-yl)methanoneHCID 10587836—
SolventDichloromethaneHCID 6344—
ProductHCID 10763869HCID 10763869—

Reaction Steps

A mixture of 1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine (0.50 g), phenylsulfonyl chloride (0.29 ml), triethylamine (0.32 ml) and dichloromethane (30 ml) is stirred at room temperature overnight. The reaction mixture is washed successively with water and saturated saline solution, and dried over magnesium sulfate. The solvent is distilled off and the resulting residue is purified by silica gel column chromatography (eluent; chloroform), and recrystallized from methanol/diethyl ether to give 1-(4-phenylsulfonylaminobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine (0.27 g) as colorless prisms, m.p. 178-182.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05985869
Source datasetuspto-grants-1999_11
ORD IDord-ad0cd1666056461d96c77cdeb08a1f7b
Source noteuspto-grants-1999_11