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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441224Generated: October 31, 2026

2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-2-one → HCID 22405146, compound

https://huagongshe.com/reaction/441224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-2-oneHCID 223771—
Reactant3,4-Dimethoxybenzenesulfonyl chlorideHCID 2734183—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 22405146HCID 2240514685%

Reaction Steps

To a solution of 1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (700 mg) in pyridine (10 ml) was added 3,4-dimethoxybenzenesulfonyl chloride (1.07 g) and the mixture was stirred at ambient temperature for 2 hours. The resulting mixture was diluted with ethyl acetate, and then the organic solution was washed successively with 0.5N hydrochloric acid, saturated aqueous sodium bicarbonate solution and brine. Drying, filtering and the removal of solvents afforded a crude product. The crude product was triturated with a mixture of diethyl ether and n-hexane (1:1) to give 5-(3,4-dimethoxybenzenesulfonyl)-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (1.33 g) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521170
Source datasetuspto-grants-1996_05
ORD IDord-f024a11c1e6b4c4cbc11b4adf77e1f4e
Source noteuspto-grants-1996_05