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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016100Generated: November 1, 2026

Phenylmethanesulfonyl chloride → N-(1-(4-(4-Chlorophenyl)piperidin-1-yl)-3-methyl-1-oxobutan-2-yl)(phenyl)methanesulfonamide

https://huagongshe.com/reaction/1016100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylmethanesulfonyl chlorideHCID 74740—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-1-(4-(4-chlorophenyl)piperidin-1-yl)-3-methylbutan-1-one hydrochlorideHCID 67299491—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductN-(1-(4-(4-Chlorophenyl)piperidin-1-yl)-3-methyl-1-oxobutan-2-yl)(phenyl)methanesulfonamideHCID 57888688—

Reaction Steps

A reaction tube was charged with benzylsulfonyl chloride (14 mg), DIEA (50 μL) and 2-amino-1-(4-(4-chlorophenyl)piperidin-1-yl)-3-methylbutan-1-one hydrochloride (20 mg) in DCM (0.3 mL). The reaction mixture was shaken overnight at rt. At the conclusion of this period, the resulting solution was diluted with MeOH and purified by preparative LC-MS to provide Example 200. MS found: (M+H)+=450.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985861B2
Source datasetuspto-grants-2011_07
ORD IDord-668ed7128d964cf8afce921b0b9e00fb
Source noteuspto-grants-2011_07