Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70327Generated: October 26, 2026

5-Bromonicotinamide → 5-(4-Formylphenyl)-3-pyridinecarboxamide

https://huagongshe.com/reaction/70327

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromonicotinamideHCID 1808—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Formylphenylboronic AcidHCID 591073—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Catalystpalladium(II) acetateHCID 167845—
Solvent1-ButanolHCID 263—
Product5-(4-Formylphenyl)-3-pyridinecarboxamideHCID 58276272—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-bromonicotinamide (0.201 g; 1.00 mmol), 4-formylphenyl boronic acid (0.180 g; 1.2 mmol), Pd(OAc)2 (0.0022 g; 0.010 mmol), S-Phos (0.0082 g; 0.020 mmol) and K2CO3 (0.345 g; 2.5 mmol) in n-butanol (3 mL) was sparged with nitrogen ca. 10 min, then heated at 80° C. for 1 h. Upon cooling, the mixture was poured into water, layered with Et2O and sonicated at room temperature ca. 5 min. Solid was collected by filtration, and the cake was air-dried on the filter, affording the title compound as a colorless solid which was used without further purification. LC/MS (method A) 1.57 min; m/z 227 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822518B2
Source datasetuspto-grants-2014_09
ORD IDord-122ab7311832496bbf3045d88ed22bcf
Source noteuspto-grants-2014_09