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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746645Generated: October 26, 2026

Lithium Hydroxide → 6-(Cyclohexylamino)pyrimidine-4-carboxylic acid

https://huagongshe.com/reaction/1746645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantTriethylamineHCID 8471—
ReactantMethyl 2-chloro-6-(cyclohexylamino)pyrimidine-4-carboxylateHCID 59447049—
ReactantHCID 68487155HCID 68487155—
ReactantEthyl 6-(cyclohexylamino)pyrimidine-4-carboxylateHCID 68488572—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthanol tetrahydrofuran waterHCID 18504229—
Product6-(Cyclohexylamino)pyrimidine-4-carboxylic acidHCID 59447075—

Reaction Steps

A mixture of methyl 2-chloro-6-(cyclohexylamino)pyrimidine-4-carboxylate (Intermediate 1, 9.20 g; 34.1 mmol), triethylamine (14.3 mL; 102 mmol) and palladium on charcoal (750 mg) in EtOH (1 L) was stirred at RT under an atmosphere of hydrogen for 16 hours. The reaction mixture was filtered through celite and the solvent was evaporated in vacuo to give a mixture of methyl 6-(cyclohexylamino)pyrimidine-4-carboxylate and ethyl 6-(cyclohexylamino)pyrimidine-4-carboxylate. This crude was dissolved in a mixture of THF/EtOH/H2O (3/2/1, 1 L) and treated with an aqueous lithium hydroxide solution (1N, 102 mmol). After 1 hour, the organic solvents were evaporated in vacuo and water was added. The aqueous layer was washed with DCM (200 mL), then acidified to pH 4 by addition of an HCl solution (1N). The aqueous layer was evaporated to reduce the volume by 30-50%. A white solid appeared and was filtered to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150519B2
Source datasetuspto-grants-2015_10
ORD IDord-3de2f7f956434e5ab390f152f29a9d8e
Source noteuspto-grants-2015_10