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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004292Generated: October 29, 2026

2-Amino-5-bromopyridine → HCID 53812896, compound

https://huagongshe.com/reaction/1004292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 53827885HCID 53827885—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 53812896HCID 53812896—

Reaction Conditions

Temperature115 °C

Reaction Steps

A mixture of 28-4 (0.3 g, 1.0 mmol), 2-amino-5-bromopyridine (0.3 g, 1.9 mmol), KOAc (0.3 g, 2.4 mmol) and Pd(OAc)2 (0.02 g, 0.1 mmol) in 6 mL DMF was purged with argon for 5 min and then heated at 90° C. for 7 hr and 115° C. for 48 hr. It was cooled, treated with 50 mL water and extracted with EtOAc (×3). The combined organic layers were washed with brine and dried over Na2SO4. After solvent removal, the residue was purified using silica gel flash chromatography (100% EtOAc to EtOAc/MeOH 10:1) to afford the desired product 28-5 as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048861
Source datasetuspto-grants-2000_04
ORD IDord-fe26211be2f441b8a0614e59ace1fc79
Source noteuspto-grants-2000_04