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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291634Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 10763869, compound

https://huagongshe.com/reaction/1291634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepineHCID 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 numberUS05753677
Source datasetuspto-grants-1998_05
ORD IDord-49e6534c57b04b6dbec4a57ea8288c71
Source noteuspto-grants-1998_05