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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889252Generated: October 29, 2026

Methanesulfonyl chloride → HCID 68432298, compound

https://huagongshe.com/reaction/889252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 68431083HCID 68431083—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 68432298HCID 68432298—

Reaction Steps

To a solution of 5-[4-(2-amino-4-methylbenzyl)-2-benzyloxy-6-fluorophenyl]-2-benzyloxymethyl-1,1-dioxo-1,2,5-thiadiazolidin-3-one (240 mg, 0.42 mmol) in pyridine (5 mL) is added methanesulfonyl chloride (0.064 mL, 0.84 mmol) and the solution is stirred at RT for 2 h. The mixture is then diluted in EtOAc, and it is washed with 1N HCl, brine and water. The organic layer is dried with MgSO4, and concentrated. The residue is purified to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252820B2
Source datasetuspto-grants-2012_08
ORD IDord-a6386251fa194d30aa2c4830767f431d
Source noteuspto-grants-2012_08