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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220207Generated: October 30, 2026

Diisopropylethylamine → [1-(2-Chloro-benzenesulfonyl)-piperidin-3-yl]-(2-m-tolyl-pyrrolidin-1-yl)-methanone

https://huagongshe.com/reaction/220207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(3-Methylphenyl)pyrrolidineHCID 3544098—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantLithium 1-(2-chloro-benzenesulfonyl)-piperidine-3-carboxylateHCID 67131265—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
SolventSodium chloride; waterHCID 57417360—
Product[1-(2-Chloro-benzenesulfonyl)-piperidin-3-yl]-(2-m-tolyl-pyrrolidin-1-yl)-methanoneHCID 5782230523.1%

Reaction Steps

To a solution 0.1 g Lithium 1-(2-chloro-benzenesulfonyl)-piperidine-3-carboxylate (0.32 mmol) in DMF: DCM (3:1) was added 0.047 g 2-(3-methyl phenyl)-pyrrolidine (0.29 mmol) and 0.27 mL DIPEA (1.6 mmol). The mixture was stirred for 10 minutes at room temperature and 0.147 g HATU (0.38 mmol) was added. The mixture was stirred overnight at room temperature, diluted with 15 mL brine and extracted with ethyl acetate (3×10 mL). The combined organic layer was dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to dryness to obtain the crude product which was further purified by column chromatography on silica eluting with 15% ethyl acetate in hexane to yield 0.03 g (20.8%) of the title compound. (MH+) 447.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202888B2
Source datasetuspto-grants-2012_06
ORD IDord-eaaebfd08dca4d62948c694e4235ded4
Source noteuspto-grants-2012_06