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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508632Generated: November 2, 2026

Dichloromethane → N-((1-(2-pivalamidoethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamide

https://huagongshe.com/reaction/508632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPivaloyl chlorideHCID 62493—
ReactantSodium BicarbonateHCID 516892—
ReactantN-((1-(2-aminoethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamideHCID 57993201—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-((1-(2-pivalamidoethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamideHCID 57993377—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of N-((1-(2-aminoethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamide (70 mg, 0.18 mmol) and TEA (123 μL, 0.881 mmol) in a 1:1 mixture of CH2Cl2:DMF (2 mL) was treated with pivaloyl chloride (42 mg, 0.35 mmol). The reaction mixture was stirred overnight then transferred to a test tube containing saturated aqueous NaHCO3 (4 mL) and EtOAc (4 mL). The biphasic mixture was mixed vigorously and allowed to separate for 15 min. After separation, the mixture was cooled to −20° C. until the aqueous layer was frozen. The organic layer was then poured off and the solvent was removed under reduced pressure at 50° C. The resulting residue was purified by HiTOPs.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096522B2
Source datasetuspto-grants-2015_08
ORD IDord-322c500364044d24b99ff00519da5809
Source noteuspto-grants-2015_08