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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276058Generated: October 26, 2026

Potassium Bicarbonate → N-benzenesulfonyl-4-acetylamino-3-(4-benzyloxybenzylamino)benzamide

https://huagongshe.com/reaction/276058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BicarbonateHCID 516893—
Reactant1-(Benzyloxy)-4-(bromomethyl)benzeneHCID 10492756—
Reactantn-Benzenesulfonyl-3-amino-4-acetylaminobenzamide potassium saltHCID 69689854—
SolventDimethylformamideHCID 6228—
ProductN-benzenesulfonyl-4-acetylamino-3-(4-benzyloxybenzylamino)benzamideHCID 18681166—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture containing 0.500 g of N-benzenesulfonyl-3-amino-4-acetylaminobenzamide potassium salt, 0.470 g of 4-benzyloxybenzyl bromide, 0.925 g of a 20% potassium hydrogencarbonate aqueous solution and 3 ml of N,N-dimethylformamide was stirred at 90° C. for 1 hour. The reaction solution was concentrated, and was purified through silica-gel column chromatography (eluent: a mixture of ethyl acetate and methanol at a ratio of 9:1) to obtain crude N-benzenesulfonyl-4-acetylamino-3-(4-benzyloxybenzylamino)benzamide. This crude product was cyclized in the same manner as in Example 183 to give 0.160 g of 6-benzenesulfonylcarbamoyl-1-(4-benzyloxybenzyl)-2-methylbenzimidazole (251).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352985B1
Source datasetuspto-grants-2002_03
ORD IDord-ad70cb05a23e43eca8c9b0b8efedb81e
Source noteuspto-grants-2002_03