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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100504Generated: October 25, 2026

2-Aminopyridine-3-carboxamide → HCID 135899198, compound

https://huagongshe.com/reaction/2100504

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminopyridine-3-carboxamideHCID 506623—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant[2-(3-Fluoro-phenyl)-ethoxy]-acetic acid methyl esterHCID 67099252—
SolventTetrahydrofuranHCID 8028—
ProductHCID 135899198HCID 13589919855%

Reaction Steps

A suspension of 2-amino-nicotinamide (250 mg, 1.82 mmol) and [2-(3-fluoro-phenyl)-ethoxy]-acetic acid methyl ester (464 mg, 2.18 mmol) in THF (5 ml) was treated with LiHMDS (1M THF solution, 4.6 ml) overnight at ambient temperature. The yellow suspension was filtrated, the filtrate was brought to dryness and the residue was purified by column chromatography (amino-phase silica gel, CH2Cl2/MeOH, 19/1) to give 2-[2-(3-fluoro-phenyl)-ethoxymethyl]-3H-pyrido[2,3-d]pyrimidin-4-one (303 mg, 1 mmol; 55%) as white solid. MS (m/e): 300.2 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572801B2
Source datasetuspto-grants-2009_08
ORD IDord-83bbf18ddbb443179660ee0a8c4a151e
Source noteuspto-grants-2009_08