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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355505Generated: November 3, 2026

Methyl 2-aminopyridine-4-carboxylate → (2-Aminopyridin-4-yl)methanol

https://huagongshe.com/reaction/1355505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-aminopyridine-4-carboxylateHCID 236984—
SolventTetrahydrofuranHCID 8028—
Product(2-Aminopyridin-4-yl)methanolHCID 1515296—

Reaction Conditions

Temperature-45 °C

Reaction Steps

2-Amino-isonicotinic acid methyl ester (6.0 g, 39.4 mmol) was dissolved in 80 mL anhydrous THF in a flame dried round bottom flask under nitrogen gas. The solution was cooled to −45° C. and LAH (39.4 mL, 1M in THF) was added slowly. The reaction was allowed to warm to 0° C. and was quenched by the addition of 15 mL of 1M NaOH (aq). The solution was filtered and the solid was washed with THF. The filtrate was concentrated to afford the pure product. 1H NMR (DMSO-d6) δ 7.79 (d, 1H, J=5.2 Hz), 6.41 (s, 1H), 6.38 (d, 1H, J=5.9 Hz), 5.79 (bs, 2H), 5.19 (t, 2H, J=5.7), 4.35 (d, 2H, J=5.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586424B2
Source datasetuspto-grants-2003_07
ORD IDord-2e68bf7c19a443fabd294575fe7f5444
Source noteuspto-grants-2003_07