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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536306Generated: October 25, 2026

Potassium Carbonate → 2-Methyl-6-[(3R)-3-[(2S)-2-methylpyrrolidin-1-yl]pyrrolidin-1-yl]-3-nitro-pyridine

https://huagongshe.com/reaction/536306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloro-2-methyl-3-nitropyridineHCID 253123—
ReactantSodium BicarbonateHCID 516892—
Reactant(2R,3'S)-2-methyl-[1,3']bipyrrolidinyl dihydrochlorideHCID 67421449—
SolventDimethyl SulfoxideHCID 679—
Product2-Methyl-6-[(3R)-3-[(2S)-2-methylpyrrolidin-1-yl]pyrrolidin-1-yl]-3-nitro-pyridineHCID 6747867798.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of (2R,3′S)-2-methyl-[1,3′]bipyrrolidinyl dihydrochloride (1.59 g, 7.0 mmol) in DMSO (24 mL) was added K2CO3 (3.87 g, 28 mmol) and 2-chloro-6-methyl-5-nitropyridine (1.81 g, 10.5 mmol) and then heated to 90° C. for 8 hours. The reaction was cooled to rt and NaHCO3 (aq) (200 mL) was added. The solution was extracted with EtOAc (2×250 mL). The combined organic extracts were washed with NaHCO3 (aq) (200 mL), H2O (200 mL), and brine (150 mL), dried over K2CO3, filtered and concentrated to afford a residue which was then purified by flash column chromatography (0% to 5% MeOH/CH2Cl2) to afford 2 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859588B2
Source datasetuspto-grants-2014_10
ORD IDord-5052441e364341508e85cec842a58dfe
Source noteuspto-grants-2014_10