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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19968Generated: October 29, 2026

Methanol → 3-Hydroxy-4-methanesulfonylamino-N-(3,4-dihydroxyphenyl)benzamide

https://huagongshe.com/reaction/19968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
Reactant3-Methoxy-4-methanesulfonylamino-N-(3,4-methylenedioxyphenyl)benzamideHCID 58703364—
SolventDichloromethaneHCID 6344—
Product3-Hydroxy-4-methanesulfonylamino-N-(3,4-dihydroxyphenyl)benzamideHCID 1167447735%

Reaction Steps

To a stirred suspension of 3-Methoxy-4-methanesulfonylamino-N-(3,4-methylenedioxyphenyl)benzamide (200 mg) in dry CH2Cl2 (20 ml) under nitrogen, was added boron tribromide (0.3 ml) then stirring continued for a further 20 hours. Methanol (50 ml) was added carefully, then the solvent evaporated in vacuo to a volume of 1 ml, this was repeated 2 more times. Purification by column chromatography over silica gel eluting with chloroform containing methanol (10-20%) gave 3-Hydroxy-4-methanesulfonylamino-N-(3,4-dihydroxyphenyl)benzamide (DC51-DB) (65 mg, 34%) as pale brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745490B2
Source datasetuspto-grants-2010_06
ORD IDord-1686814b05de4bdab2ffcff5ed7dbd2a
Source noteuspto-grants-2010_06