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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467080Generated: October 30, 2026

Methanesulfonyl chloride → HCID 19813442, compound

https://huagongshe.com/reaction/467080

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 numberUS05158964
Source datasetuspto-grants-1992_10
ORD IDord-dc1dbe1c6f7946f190ce07755cea1a14
Source noteuspto-grants-1992_10