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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016093Generated: October 31, 2026

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

https://huagongshe.com/reaction/1016093

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 numberUS07985861B2
Source datasetuspto-grants-2011_07
ORD IDord-389a42b0707243d6bef34c724bbbacf7
Source noteuspto-grants-2011_07