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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375986Generated: November 1, 2026

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

https://huagongshe.com/reaction/2375986

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 numberUS07465731B2
Source datasetuspto-grants-2008_12
ORD IDord-d8b2198e33db4b249467886fd2b45271
Source noteuspto-grants-2008_12