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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351270Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86592860, compound

https://huagongshe.com/reaction/351270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 91605231HCID 91605231—
SolventTriethylamineHCID 8471—
ProductHCID 86592860HCID 8659286081.3%

Reaction Steps

To a solution of tert-butyl{4-[3-(1-hydroxy-1-methyl-ethyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]benzyl}-carbamate (1.1 g) and Et3N (1.02 g) was added methane sulfonyl chloride (576 mg). The mixture was stirred at ambient temperature overnight. The mixture was concentrated in vacuo. The residue was partitioned between AcOEt and 1M HCl. The organic layer was separated, washed with saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography eluted with AcOEt/n-hexane=25%. The pure fraction was collected and concentrated in vacuo to give tert-butyl {4-[3-isopropenyl-1-(4-methoxyphenyl)-1-H-pyrazol-5-yl]benzyl}carbamate (857 mg) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183306B2
Source datasetuspto-grants-2007_02
ORD IDord-829e12dd1f7842a691ae85fb024600c3
Source noteuspto-grants-2007_02