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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945428Generated: November 2, 2026

Methyl 2-aminopyridine-4-carboxylate → HCID 24811989, compound

https://huagongshe.com/reaction/1945428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-aminopyridine-4-carboxylateHCID 236984—
ReactantPMID26882240-Compound-8HCID 625381—
ReactantPyBOPHCID 2724699—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 24811989HCID 2481198975.5%

Reaction Steps

To a solution of appropriate (4-adamantan-1-yl-phenoxy)-acetic acid (150 mg, 0.523 mmol), 2-amino isonicotinic acid methyl ester (159.3 mg, 1.04 mmol) and DMAP (127.9 mg, 1.04 mmol) in DMF (6 ml) was added PyBOP (545 mg, 1.04 mmol) at room temperature and the resulting mixture was stirred until reaction completion as indicated by TLC. Reaction mixture was poured onto ice cold water, diluted with ethyl acetate, separated organic layer and sequentially washed with aqueous sodium bicarbonate, brine and water, and dried over anhydrous MgSO4. The solvent was filtered and evaporated under reduced pressure to afford a crude solid, which was purified by flash chromatography on silica gel (EtOAc:hexanes=1:9 to 1:1) to afford of 2-[2-(4-adamantan-1-yl-phenoxy)acetylamino]-isonicotinic acid methyl ester as a colorless solid (0.166 g, 75% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394799B2
Source datasetuspto-grants-2013_03
ORD IDord-d902aca7166240b39eb5f6d4dc86bfaa
Source noteuspto-grants-2013_03