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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454692Generated: October 30, 2026

Methanesulfonyl chloride → HCID 66991255, compound

https://huagongshe.com/reaction/454692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 66990307HCID 66990307—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 66991255HCID 66991255—

Reaction Steps

Under ice-cooling, methanesulfonyl chloride (0.018 mL) was added to a solution mixture of methyl 2-(2-(benzyloxy)-5-(2-(piperazin-1-yl)ethoxy)benzamido)-4-phenylbenzoate (0.11 g) in methylene chloride (2.2 mL) and pyridine (0.024 mL), followed by stirring at room temperature for 1 hour. Pyridine (0.016 mL) and methanesulfonyl chloride (9.0 μL) were sequentially added to the reaction mixture, followed by stirring at room temperature for 1 hour and 30 minutes. The solvent was evaporated under reduced pressure, and a saturated aqueous solution of sodium bicarbonate and ethyl acetate were added to the residue. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [Kanto Chemical Co., Inc., silica gel 60 (spherical), eluent: 50-0% hexane/ethyl acetate] to obtain 0.085 g of methyl 2-(2-(benzyloxy)-5-(2-(4-(methylsulfonyl)piperazin-1-yl)ethoxy)benzamido)-4-phenylbenzoate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-408d7661c14a4379b98206b0ced016c5
Source noteuspto-grants-2013_07