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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226299Generated: October 30, 2026

Ethyl Acetate → methyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}nicotinate

https://huagongshe.com/reaction/226299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 6-chloropyridine-3-carboxylateHCID 254249—
Reactant(3R)-1-benzylpyrrolidin-3-amineHCID 1519354—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productmethyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}nicotinateHCID 6896048168.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of methyl 6-chloronicotinate (8.0 g), (3R)-(−)-1-benzyl-3-aminopyrrolidine (9.86 g), CuO (371 mg) and K2CO3 (8.38 g) in DMF (60 ml) was stirred at 100° C. for 10 hours under atmospheric pressure of nitrogen. The reaction mixture was poured into a mixture of AcOEt and water and the organic layer was washed with brine and dried over MgSO4. The solvent was evaporated in vacuo and the residue was chromatographed on silicagel eluting with AcOEt-MeOH (97:3). The eluted fractions containing the desired product were collected and evaporated in vacuo to give methyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}nicotinate (9.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-0b7801fae5c7464889045bca4c81d6b0
Source noteuspto-grants-2009_07