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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820163Generated: October 30, 2026

1,2-Dichloroethane → N-(1-(4-(4-chlorophenyl)piperidin-1-yl)-3-methyl-1-oxobutan-2-yl)-2-phenylacetamide

https://huagongshe.com/reaction/1820163

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantPhenylacetic AcidHCID 999—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-Amino-1-(4-(4-chlorophenyl)piperidin-1-yl)-3-methylbutan-1-one hydrochlorideHCID 67299491—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventDiisopropylethylamineHCID 81531—
ProductN-(1-(4-(4-chlorophenyl)piperidin-1-yl)-3-methyl-1-oxobutan-2-yl)-2-phenylacetamideHCID 24758856—

Reaction Steps

A reaction tube was charged with HOBt (10 mg), phenylacetic acid (12 mg) and EDC (14 mg) in DMF (0.7 mL). The resulting mixture was agitated at rt. for 15 min, and then a solution of 2-amino-1-(4-(4-chlorophenyl)piperidin-1-yl)-3-methylbutan-1-one hydrochloride (20 mg) in DIEA (50 μL) and DMF (250 μL) was added and the resulting 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 9. MS found: (M+H)+=414.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601844B2
Source datasetuspto-grants-2009_10
ORD IDord-59b3d913929847189f1a3af549b9fa13
Source noteuspto-grants-2009_10