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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952215Generated: November 2, 2026

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

https://huagongshe.com/reaction/1952215

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 numberUS08404848B2
Source datasetuspto-grants-2013_03
ORD IDord-22becd4dbb10407cb3bdac8ea6b00345
Source noteuspto-grants-2013_03