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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377221Generated: October 27, 2026

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

https://huagongshe.com/reaction/377221

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 (.Yen.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 numberUS06025366
Source datasetuspto-grants-2000_02
ORD IDord-3465bd294fce4eaca68cb7e49179caa4
Source noteuspto-grants-2000_02