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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746646Generated: October 31, 2026

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

https://huagongshe.com/reaction/1746646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantTriethylamineHCID 8471—
ReactantMethyl 6-(cyclopentylamino)pyrimidine-4-carboxylateHCID 67528393—
ReactantEthyl 6-(cyclopentylamino)pyrimidine-4-carboxylateHCID 67529171—
ReactantHCID 86644304HCID 86644304—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthanol tetrahydrofuran waterHCID 18504229—
Product6-(Cyclopentylamino)pyrimidine-4-carboxylic acidHCID 59447055—

Reaction Steps

A mixture of methyl 2-chloro-6-[(cyclopentylmethyl)amino]pyrimidine-4-carboxylate (Intermediate 2, 2.00 g; 7.82 mmol; 1.00 eq.), palladium on charcoal (750 mg) and triethylamine (3.27 mL; 23.5 mmol) in EtOH (200 mL) was stirred under an atmosphere of hydrogen for 2 hours. After 2 hours the reaction mixture was filtered on celite and evaporated to give a mixture of methyl 6-(cyclopentylamino)pyrimidine-4-carboxylate and ethyl 6-(cyclopentylamino)pyrimidine-4-carboxylate. The crude mixture was dissolved in a mixture of THF/EtOH/H2O (3/2/1, 120 mL) and treated with an aqueous solution of lithium hydroxide (1N, 23.5 mL, 23.5 mmol). The reaction mixture was stirred at RT for 60 minutes. Water was added (50 mL) and the aqueous layer was washed with DCM (30 mL). The aqueous layer was acidified to pH 5 by addition of an HCl solution (1N). The aqueous layer was evaporated in vacuo to reduce the volume by 30-50%. The resulting white solid 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-ff3085315da44194bcf5dbeb1e6a8c53
Source noteuspto-grants-2015_10