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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031961Generated: November 1, 2026

Methanesulfonyl chloride → HCID 10433970, compound

https://huagongshe.com/reaction/1031961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 15735403HCID 15735403—
SolventPyridineHCID 1049—
ProductHCID 10433970HCID 10433970—

Reaction Steps

Methanesulphonyl chloride (0.76 g, 6.6 mmole) was added dropwise to a solution of N-methyl-N-(5-aminobenzofur-2-ylmethyl)-4-aminophenethylamine (see Preparation 3--0.9 g, 3.0 mmole) in pyridine (25 ml) and the mixture was stirred at room temperature for 18 hours. The solvent was then evaporated and the residue diluted with aqueous sodium bicarbonate and extracted three times with methylene chloride. The combined organic extracts were dried (MgSO4) and evaporated, and the residue was purified by chromatography on silica eluting with ethyl acetate. The product-containing fractions were combined, evaporated and the resulting solid was recrystallised from ethyl acetate/methanol to give the title compound, yield 0.35 g, m.p. 177°-179°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04956382
Source datasetuspto-grants-1990_09
ORD IDord-9bc2fd5b2b9f40a1aa716a29ae0fb475
Source noteuspto-grants-1990_09