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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201707Generated: October 29, 2026

Sodium Bicarbonate → N-(2-amino-5-(pyridin-3-yl)phenyl)pyrrolidine-1-carboxamide

https://huagongshe.com/reaction/2201707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3-Pyridinylboronic acidHCID 2734378—
ReactantN-(2-amino-5-bromophenyl)pyrrolidine-1-carboxamideHCID 86712537—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-amino-5-(pyridin-3-yl)phenyl)pyrrolidine-1-carboxamideHCID 7146638168.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of N-(2-amino-5-bromophenyl)pyrrolidine-1-carboxamide (0.26 g, 0.72 mmol) in THF (10 mL) and water (5 mL) were added pyridin-3-ylboronic acid (0.13 g, 1.07 mmol, 1.5 equiv.), sodium bicarbonate (0.11 g, 1.07 mmol, 1.5 equiv.) and palladium(0) (0.08 g, 0.07 mmol, 0.1 equiv.). The reaction mass was stirred at 90° C. for sixteen hours. The reaction crude was filtered on a celite bed and diluted in ethyl acetate. The organic layers were washed with water and brine then dried over Na2SO4 and concentrated. The residue was purified by column chromatography on eluting ethyl acetate and hexane to allow N-(2-amino-5-(pyridin-3-yl)phenyl)pyrrolidine-1-carboxamide (0.14 g, 63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365498B2
Source datasetuspto-grants-2016_06
ORD IDord-2f7fc84e83604e9897f456091a5c05e2
Source noteuspto-grants-2016_06