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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741256Generated: October 30, 2026

Water → 221298-62-0

https://huagongshe.com/reaction/1741256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 11007933HCID 11007933—
Reactant2,3-Pyridinedicarboxylic acid, 5-methyl-, 2,3-dimethyl esterHCID 11745869—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTolueneHCID 1140—
Product221298-62-0HCID 1147135268.6%

Reaction Steps

A stirred mixture of dimethyl 5-methylpyridine-2,3-dicarboxylate (52.25 g, 0.25 mol) and (R)2-amino-2,3-dimethylbutyramide (33.43 g, 0.2563 mol, 96.2% R isomer) in dry toluene is treated with KOt-Bu (29.4 g, 0.2625 mol) at 35° C., stirred at ambient temperatures for 10 minutes, treated with a second portion of KOt-Bu (29.4 g, 0.2625 mol) at 40° C., heated at 80°-85° C. for 1.5-2.0 hr, cooled to room temperature, treated with water and stirred until dissolution of solids is complete. The phases are separated. The aqueous phase is acidified to pH 3 with concentrated HCl, stirred at pH 3 for 10-15 min., and filtered. The aqueous filtrate is extracted with methylene chloride. The filtercake is dispersed in methylene chloride and the dispersion is filtered. The methylene chloride extracts and the methylene chloride filtrate are combined, dried over MgSO4 and concentrated to dryness in vacuo to give the title product as a white solid, 47.3 g, 68.6% yield, 98.1% pure, 97% R isomer by quantitative NMR analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05973154
Source datasetuspto-grants-1999_10
ORD IDord-5601706a07124fc0bfc3aa5956a95115
Source noteuspto-grants-1999_10