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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490967Generated: October 30, 2026

Sodium Carbonate → 5-(4-Fluorophenyl)pyridine-3-carboxylic acid morpholinamide

https://huagongshe.com/reaction/490967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactant5-Bromonicotinic acid morpholinamideHCID 69528427—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-(4-Fluorophenyl)pyridine-3-carboxylic acid morpholinamideHCID 6952900993%

Reaction Conditions

Temperature65 °C

Reaction Steps

1.2 g of Pd[P(Ph)3]4 and 7.6 g of p-fluorobenzeneboronic acid are added to a solution of 14.3 g of 5-bromonicotinic acid morpholinamide in 100 g of THF. A solution of 8.0 g of Na2CO3 in 25 g of water is subsequently added dropwise with stirring at 65° C. After 16 hours, the reaction mixture is cooled and evaporated in a rotary evaporator. The residue is taken up in dichloromethane, activated carbon is added, and the mixture is filtered. Repeated extraction of the filtrate with water and evaporation in a rotary evaporator gives a residue of 15.7 g, which, according to HPLC, comprises 89% of 5-(4-fluorophenyl)pyridine-3-carboxylic acid morpholinamide (net yield 93% of theory). Recrystallisation from ethyl acetate gives 8.0 g of 5-(4-fluorophenyl)pyridine-3-carboxylic acid morpholinamide having an HPLC purity of 99.6% (53.3% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528256B2
Source datasetuspto-grants-2009_05
ORD IDord-f83d971deb4045518f110f7e9e19ada6
Source noteuspto-grants-2009_05