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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226300Generated: October 26, 2026

Ethyl Acetate → ethyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloronicotinate

https://huagongshe.com/reaction/226300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant(3R)-1-benzylpyrrolidin-3-amineHCID 1519354—
ReactantEthyl 5,6-DichloronicotinateHCID 16762519—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productethyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloronicotinateHCID 6896768697.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of ethyl 5,6-dichloronicotinate (10.0 g), (3R)-(−)-1-benzyl-3-aminopyrrolidine (9.61 g), K2CO3 (8.38 g) and CuO (371 mg) 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-n-Hexane (7:3). The eluted fractions containing the desired product were collected and evaporated in vacuo to give ethyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloronicotinate (15.95 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-354e60262bf74c718f757758f5b4485b
Source noteuspto-grants-2009_07