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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360632Generated: November 1, 2026

Methyl 5-aminopyridine-3-carboxylate → (5-Aminopyridin-3-yl)methanol

https://huagongshe.com/reaction/2360632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-aminopyridine-3-carboxylateHCID 1514432—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(5-Aminopyridin-3-yl)methanolHCID 29921874—

Reaction Steps

5-Amino-nicotinic acid methyl ester (5.7 g, 30.2 mmol) was dissolved in THF (150 ml) and LiAlH4 (1M in THF solution 133 ml, 133 mmol) added slowly at 0° C. The reaction mixture was stirred at room temperature for 21 h. The reaction mixture was quenched and acidified to pH 3 using dilute HCl, and basified (pH 8) using solid Na2CO3. Solvents were removed under reduced pressure. The residue was filtered through silica gel using 20% MeOH/DCM yielding the product 3.8 g, (100%) with LCMS purity 97%, m/z 125 [M++H]+, by ELS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686032B2
Source datasetuspto-grants-2014_04
ORD IDord-fcc3555f29794cafa9e70e30bf0d6f85
Source noteuspto-grants-2014_04