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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621990Generated: October 29, 2026

Benzenesulfinic acid → HCID 66599996, compound

https://huagongshe.com/reaction/1621990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfinic acidHCID 12057—
ReactantSodium HydroxideHCID 14798—
ReactantL-ProlineHCID 145742—
Reactant3-Amino-5-bromopyridineHCID 817681—
ReactantSodiumHCID 5360545—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 66599996HCID 6659999611%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 5-bromopyridin-3-amine (1.59 g, 9.19 mmol) (Aldrich) was added benzenesulfinic acid, sodium salt (1.810 g, 11.03 mmol) (Sigma-Aldrich), copper(I) iodide (0.175 g, 0.919 mmol), (S)-pyrrolidine-2-carboxylic acid (0.212 g, 1.838 mmol), sodium hydroxide (0.074 g, 1.838 mmol), and DMSO (18 mL), and the resulting mixture was stirred at 100° C. for 3 days. The reaction mixture was then diluted with 200 mL of EtOAc, added to a separatory funnel, and partitioned with sodium bicarbonate (saturated, aqueous). The organic layer was separated, washed 4 times with 150 mL of sodium bicarbonate (saturated, aqueous), dried over sodium sulfate, and concentrated in vacuo. Chromatographic purification of the residue (silica gel, 0% to 3% (2 M ammonia in MeOH)/DCM) furnished the title compound (11% yield). m/z (ESI, +ve ion) 235.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772480B2
Source datasetuspto-grants-2014_07
ORD IDord-2cb1ab22f21e4ec1bf8070436d168be2
Source noteuspto-grants-2014_07