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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489958Generated: November 3, 2026

Methanesulfonyl chloride → HCID 131723416, compound

https://huagongshe.com/reaction/489958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 178478002HCID 178478002—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductHCID 131723416HCID 13172341637%

Reaction Steps

A solution of 3-(4-chlorophenyl)-4-(4-pyridyl)-5-(4-piperazinyl)pyrazole (200 mg; 0.54 mmol; prepared as set forth in Example A-169), methanesulfonyl chloride (75 mg) and 4-dimethylaminopyridine (5 mg) in pyridine was stirred at room temperature for 3 hours. The solvent was removed in vacuo and the residue was treated with water. The resultant crystalline solid was filtered, air dried and recrystallized from methanol and water to give 118 mg (37%) of 1-[5-(4-chlorophenyl)-4-(4-pyridinyl)-1H-pyrazol-3-yl]-4-(methylsulfonyl)piperazine, monohydrate, m.p. 245-248° C. Anal. Calc'd. for C19H20ClN5SO2.H2O: C, 52.35; H, 5.09; N, 16.07. Found: C, 52.18; H, 5.31; N, 16.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979686B1
Source datasetuspto-grants-2005_12
ORD IDord-a53bdf209d154ac5a8449540b4856f26
Source noteuspto-grants-2005_12