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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636053Generated: October 30, 2026

Methanesulfonyl chloride → HCID 23383640, compound

https://huagongshe.com/reaction/1636053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 22743447HCID 22743447—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 23383640HCID 23383640—

Reaction Steps

N,N-dimethyl-4-pyridinamine (0.01062 mol) and intermediate 5a (0.00708 mol) were suspended in CH2Cl2 (50 ml). A solution of methanesulfonylchloride (0.01062 mol) in CH2Cl2 (30 ml) was added dropwise at room temperature. The mixture was stirred at room temperature for the weekend. N,N-dimethyl-4-pyridinamine (0.00352 mol) and methanesulfonylchloride (0.00358 mol) were added again. The mixture was stirred overnight, washed with water (2×100 ml), dried, filtered over decalite and the solvent was evaporated. The residue was dissolved in MIK (150 ml). Activated charcoal (0.5 g) was added. The mixture was boiled, filtered warm and stirred for 2 hours. The precipitate was filtered off and dried, yielding 1.7 g (50%) of [S-(R*,S*)]-2,4-dihydro-2-(2-methanesulfonyloxy-1-methylpropyl)-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-3H-1,2,4-triazol-3-one (interm. 5d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06512116B2
Source datasetuspto-grants-2003_01
ORD IDord-9b9ff6fb6b274819928adbe8dc6e0bf9
Source noteuspto-grants-2003_01