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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388768Generated: October 26, 2026

2,6-Lutidine → N-((1-(2-(1-methylethylsulfonamido)ethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamide

https://huagongshe.com/reaction/388768

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
Reactant2-Propanesulfonyl chlorideHCID 82408—
ReactantSodium BicarbonateHCID 516892—
ReactantN-((1-(2-aminoethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamideHCID 57993201—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-((1-(2-(1-methylethylsulfonamido)ethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamideHCID 57993269—

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 2,6-lutidine (123 μL, 0.882 mmol) in CH2Cl2 (2 mL) was treated with isopropylsulfonyl chloride (49.9 mg, 0.35 mmol). The reaction was stirred overnight and then transferred to a test tube containing saturated aqueous NaHCO3 (4 mL) and EtOAc (4 mL). The biphasic mixture was mixed vigourously 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 numberUS08377968B2
Source datasetuspto-grants-2013_02
ORD IDord-beb4f1eb39b34aa59b00e09638ee17cd
Source noteuspto-grants-2013_02