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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895899Generated: October 31, 2026

Diisopropylethylamine → 2-(1-(3-(Trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione

https://huagongshe.com/reaction/1895899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
Reactant2-(Piperidin-4-yloxy)isoindoline-1,3-dione trifluoroacetic acidHCID 67118385—
SolventDichloromethaneHCID 6344—
Product2-(1-(3-(Trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dioneHCID 6711838693%

Reaction Steps

3-(Trifluoromethyl)benzenesulfonyl chloride (3.23 g, 13.2 mmol) was added to a solution of 2-(piperidin-4-yloxy)isoindoline-1,3-dione trifluoroacetic acid (3.56 g, 9.80 mmol) and N,N-diisopropylethylamine (7.10 g, 55.0 mmol) in CH2Cl2 (85 ml), and stirred at room temperature for 17 hours. The reaction mixture was washed with aqueous 1 N HCl solution (20 ml×3), aqueous NaHCO3 solution (20 ml×3), brine (20 ml×2), dried over Na2SO4, filtered and concentrated in vacuo to give 2-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione (4.12 g, 93%) as a white solid: LCMS: 454 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518934B2
Source datasetuspto-grants-2013_08
ORD IDord-0ed696eadb294aa28429dd3271a297fb
Source noteuspto-grants-2013_08