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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69715Generated: October 25, 2026

L-Proline, ethyl ester → (S)-ethyl 1-(5-bromo-3-nitropyridin-2-yl)pyrrolidine-2-carboxylate

https://huagongshe.com/reaction/69715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Proline, ethyl esterHCID 79888—
Reactant5-Bromo-2-chloro-3-nitropyridineHCID 7019412—
Product(S)-ethyl 1-(5-bromo-3-nitropyridin-2-yl)pyrrolidine-2-carboxylateHCID 5832435698%

Reaction Conditions

Temperature90 °C

Reaction Steps

5-bromo-2-chloro-3-nitropyridine (5.94 g, 25 mmol) and (S)-ethyl pyrrolidine-2-carboxylate (7.52 g, 52.5 mmol) were combined and stirred at 90° C. for 10 min in a closed vial. The crude material was purified by flash column chromatography (20-30% EtOAc in hexanes to afford (S)-ethyl 1-(5-bromo-3-nitropyridin-2-yl)pyrrolidine-2-carboxylate (8.43 g, 24.49 mmol, 98% yield) as a yellow viscous oil. [M+H] calc'd for C12H14BrN3O4, 344; found, 344.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822470B2
Source datasetuspto-grants-2014_09
ORD IDord-bb4a549c5f6f4e35b9cca064c95a6699
Source noteuspto-grants-2014_09