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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420622Generated: November 1, 2026

Water → Methyl 1-Acetyl-4-(4-hydroxybenzenesulfonyl)-2,3,4,5-tetrahydro-1H-[1,4]benzodiazepine-3-carboxylate

https://huagongshe.com/reaction/1420622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoron tribromideHCID 25134—
ReactantHCID 18612735HCID 18612735—
SolventDichloromethaneHCID 6344—
ProductMethyl 1-Acetyl-4-(4-hydroxybenzenesulfonyl)-2,3,4,5-tetrahydro-1H-[1,4]benzodiazepine-3-carboxylateHCID 1861278277.6%

Reaction Steps

To a cooled (0°) solution of 2.0 g (4.78 mmol) of methyl 1-acetyl-4-(4-methoxybenzenesulfonyl)-2,3,4,5-tetrahydro-1H-[1,4]benzodiazepine-3-carboxylate in 14 ml of CH2Cl2 was added dropwise 143.3 ml (14.3 mmol) of a 1.0 molar solution of BBr3 in CH2Cl2The mixture was stirred at room temperature for 1.5 hours. Ice and H2O were added to the reaction mixture and the insolubles filtered off. The filtrate was diluted with CH2Cl2 and H2O and the CH2Cl2 layer separated, washed with brine and dried (Na2SO4) The solvent was removed under vacuum to give 1.5 g of a white foam. The solid was chromatographed on silica gel with hexane-ethyl acetate (1:1) as solvent to give a foam which was dried under vacuum to give 0.52 g of product as a white foam; Anal. Calc'd for C19H20N2O6S: C, 56 4:H, 5.0; N, 6.9 Found: C 55.1; H, 4.7: N, 6.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071903
Source datasetuspto-grants-2000_06
ORD IDord-dbb8196a974648268c6dac681b95c806
Source noteuspto-grants-2000_06