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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052013Generated: October 30, 2026

Hydrochloric Acid → 4-(3-Oxopyrrolidin-1-yl)-pyridine-2-carboxylic acid phenylamide

https://huagongshe.com/reaction/1052013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroformHCID 6212—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(3-Hydroxypyrrolidin-1-yl)-pyridine-2-carboxylic acid phenylamideHCID 86695827—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Product4-(3-Oxopyrrolidin-1-yl)-pyridine-2-carboxylic acid phenylamideHCID 8669582850%

Reaction Steps

A solution of 4-(3-Hydroxypyrrolidin-1-yl)-pyridine-2-carboxylic acid phenylamide (259 mg, 0.92 mmol) in dichloromethane (5 mL) and dimethylsulfoxide (2.5 mL) was cooled in an ice bath. Diisopropylethylamine (0.48 mL, 2.8 mmol) was added and stirred for 5 minutes. A solution of sulfur trioxide-pyridine complex (0.44 g, 2.8 mmol) in DMSO (2.5 mL) was added dropwise. The reaction was stirred at 0° C. for 3 hours. To the reaction was added 1 M hydrochloric acid (6 mL) and chloroform. The layers were separated. The aqueous layer was treated with saturated aqueous sodium bicarbonate until pH=6. Extraction twice with chloroform gave a crude residue. Purification by chromatography on silica gel (12 g) eluted with chloroform:methanol 39:1 gave the title compound (133 mg, 0.46 mmol, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388176B2
Source datasetuspto-grants-2016_07
ORD IDord-3cb8cd27f2884d35b7a873fa070caa7b
Source noteuspto-grants-2016_07