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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976701Generated: October 31, 2026

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

https://huagongshe.com/reaction/1976701

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 (x3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue (31.6 g) 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 numberUS06228867B1
Source datasetuspto-grants-2001_05
ORD IDord-d1bb76d8e97340819762033aef204693
Source noteuspto-grants-2001_05