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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600629Generated: October 30, 2026

Ethyl Acetate → 2-(6-Aminopyridin-3-yl)propan-2-ol

https://huagongshe.com/reaction/600629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 6-aminonicotinateHCID 737487—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Product2-(6-Aminopyridin-3-yl)propan-2-olHCID 59473771—

Reaction Steps

To a solution of 0.7 g of methyl 6-aminonicotinate in 65 mL of THF, cooled to 10° C. and under argon, are added dropwise 15 mL of a 3M solution of methylmagnesium chloride in THF. The reaction mixture is stirred for 15 hours, while allowing the temperature to rise to 20° C., and is then cooled again in an ice bath. 100 mL of saturated ammonium chloride solution and then 200 mL of ethyl acetate are added slowly. The organic phase is dried and concentrated to dryness. The residue is taken up in ethyl acetate. The precipitate is filtered off by suction and dried to give 0.4 g of 2-(6-aminopyridin-3-yl)propan-2-ol in the form of a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902219B2
Source datasetuspto-grants-2011_03
ORD IDord-13ab20eb2c00429ab4850ab6beff6d24
Source noteuspto-grants-2011_03