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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645375Generated: October 29, 2026

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

https://huagongshe.com/reaction/645375

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

15 ml of a 3M solution of methylmagnesium chloride in THF are added dropwise to a solution, cooled to 10° C. and under argon, of 0.7 g of methyl 6-aminonicotinate in 65 ml of THF. The reaction mixture is stirred for 15 h, while allowing the temperature to rise to 20° C., and then again cooled in an ice bath. 100 ml of a saturated ammonium chloride solution and then 200 ml of ethyl acetate are slowly added. The organic phase is dried and concentrated to dryness. The residue is taken up in ethyl acetate. The precipitate is filtered off 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 numberUS07704989B2
Source datasetuspto-grants-2010_04
ORD IDord-d9948faaa43a44b98bbd66fdba04ba95
Source noteuspto-grants-2010_04