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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637193Generated: November 2, 2026

Methanesulfonyl chloride → HCID 19347999, compound

https://huagongshe.com/reaction/1637193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 19347997HCID 19347997—
SolventDichloromethaneHCID 6344—
ProductHCID 19347999HCID 1934799966.2%

Reaction Steps

Methanesulfonyl chloride (0.043 ml, 0.55 mmol) was added to a stirred solution of ethyl 6-(hydroxymethyl)-3-[(3-methoxyphenyl)sulfinyl]benzo[b]thiophene-2-carboxylate (Preparation 17, 195 mg, 0.5 mmol) and N-ethyl-N,N-diisopropylamine (0.1 ml, 0.55 mmol) in dichloromethane (3 ml) at 0° C. After 3 hours the solution was washed twice with water, dried (magnesium sulfate), and the solvent removed under reduced pressure. The residue was crystallised from diethyl ether to give the title compound as a colourless solid (155 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040309
Source datasetuspto-grants-2000_03
ORD IDord-dcdb52a804d142059094f8e1d224c8a9
Source noteuspto-grants-2000_03