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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345022Generated: October 30, 2026

Methanesulfonyl chloride → HCID 19813442, compound

https://huagongshe.com/reaction/345022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 19813432HCID 19813432—
SolventPyridineHCID 1049—
ProductHCID 19813442HCID 19813442—

Reaction Steps

Methanesulphonyl chloride (0.21 g, 1.85 mmole) was added dropwise to a solution of N-methyl-N-(3-methyl-5-aminobenzofur-2-ylmethyl)-4-methanesulphonamidophenethylamine (see Preparation 10B - 0.78 g, 1.68 mmole) in pyridine (7 ml) and the solution was then stirred at room temperature for 60 hours. The solvent was evaporated and the residue triturated with toluene. The toluene was decanted, the residue stirred with aqueous sodium bicarbonate, and the precipitate collected by filtration and recrystallised from methanol to give the title compound, yield 0.38 g, m.p. 142°-143.5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055473
Source datasetuspto-grants-1991_10
ORD IDord-1bd76241bd0b47a6a9dd3a8dec90aa5d
Source noteuspto-grants-1991_10