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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401102Generated: October 31, 2026

Potassium Carbonate → (2S,3'S)-2-Methyl-1'-(6-methyl-5-nitro-pyridin-2-yl)-[1,3']bipyrrolidinyl

https://huagongshe.com/reaction/2401102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloro-2-methyl-3-nitropyridineHCID 253123—
Reactant(2S,3'S)-2-Methyl-[1,3']bipyrrolidinyl dihydrochlorideHCID 67422681—
SolventAcetonitrileHCID 6342—
Product(2S,3'S)-2-Methyl-1'-(6-methyl-5-nitro-pyridin-2-yl)-[1,3']bipyrrolidinylHCID 7128093882.6%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of (2S,3′S)-2-methyl-[1,3′]bipyrrolidinyl dihydrochloride (0.596 g, 2.64 mmol,) in acetonitrile (25 mL) was added 2-chloro-5-nitro-6-picoline (0.685 g, 3.96 mmol,) and powder potassium carbonate (1.45 g, 10.6 mmol), then heated to 65° C. for 4.0 hr, then at 45° C. for 16 hr. The reaction mixture was then allowed to cool to room temperature and filtered through a 10 g Varian Bond Elut SCX (strong cation-exchange) cartridge eluting with 50 mL of (1:1) methanol in dichloromethane, 25 mL of methanol, followed by 7N ammonia in methanol (50 mL). The filtrate was concentrated under vacuum, to afford 0.633 g (82%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796278B2
Source datasetuspto-grants-2014_08
ORD IDord-7732649dba0f4e83a00682e8241f069c
Source noteuspto-grants-2014_08