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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421512Generated: October 27, 2026

Methanol → Methyl 2-(6-aminopyridin-3-yl)-2-methylpropanoate

https://huagongshe.com/reaction/1421512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant2-(6-Aminopyridin-3-yl)-2-methylpropanoic acid hydrochlorideHCID 67130849—
ProductMethyl 2-(6-aminopyridin-3-yl)-2-methylpropanoateHCID 21998700—

Reaction Steps

A solution of 2-(6-aminopyridin-3-yl)-2-methylpropanoic acid hydrochloride (35.0 g, 0.162 mmol) and concentrated H2SO4 (5 mL) in MeOH (250 mL) was heated at reflux overnight. After cooling to ambient temperature, the reaction was quenched cautiously with saturated aqueous NaHCO3 and concentrated in vacuo. The residue was partitioned between ethyl acetate and water, the organic phase separated and the aqueous phase re-extracted with ethyl acetate (×3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue (31.6 g, 100%) was judged pure by a combination of TLC and 1H nmr analysis and was used without further purification in the subsequent reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06077847
Source datasetuspto-grants-2000_06
ORD IDord-47a6db70ea2648d9a9e96b4028c7c460
Source noteuspto-grants-2000_06