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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117368Generated: November 1, 2026

Methanesulfonyl chloride → HCID 12069574, compound

https://huagongshe.com/reaction/2117368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 12069573HCID 12069573—
SolventPyridineHCID 1049—
ProductHCID 12069574HCID 1206957475.1%

Reaction Steps

0.292 ml (3.78 mmol) of mesyl chloride is added to a solution of 350 mg (1.08 mmol) of the compound of Example 29 in 3 ml of pyridine, and the medium is stirred at room temperature for 4 hours. The reaction medium is concentrated under reduced pressure. The residue is taken up in 1 N hydrochloric acid and extracted with dichloromethane. The organic phase is separated after settling out, washed with a saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated under reduced pressure. The residue is crystallized from ethanol. 327 mg of yellow crystals are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442708B2
Source datasetuspto-grants-2008_10
ORD IDord-5b821cdb49b544b89fb979b7eab03348
Source noteuspto-grants-2008_10