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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517619Generated: October 25, 2026

Hydrochloric Acid → Methyl 2-(6-chloro-2-methylpyrimidin-4-yl-amino)thiazol-5-carboxylic acid

https://huagongshe.com/reaction/517619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant4,6-Dichloro-2-methylpyrimidineHCID 234997—
Reactant2-Amino-4-methyl-thiazole-5-carboxylic acidHCID 832243—
SolventTetrahydrofuranHCID 8028—
SolventDimethylacetamideHCID 31374—
ProductMethyl 2-(6-chloro-2-methylpyrimidin-4-yl-amino)thiazol-5-carboxylic acidHCID 11831926987.3%

Reaction Steps

In a reaction flask, 49.49 g 4,6-dichloro-2-methylpyrimidine (0.303 mol), 40.00 g methyl 2-aminothiazol-5-carboxylic acid (0.253 mol), and 200 ml N,N-dimethylacetamide were charged, the temperature was brought to −5° C. and 18.20 g sodium hydride (0.455 mol) in 90 ml tetrahydrofuran were added dropwise and the reaction mixture was kept under these conditions for about three hours. At the end of the reaction, 250 ml of a solution of hydrochloric acid 2N were added, the temperature was brought to the room value, the formed solid was filtered and washed with water (4×200 ml) and dried in oven under vacuum at a temperature of 55° C. for about eight hours, to give 62.89 g methyl 2-(6-chloro-2-methylpyrimidin-4-yl-amino)thiazol-5-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115124B1
Source datasetuspto-grants-2015_08
ORD IDord-c6b4fa359e61427087f2bde4f7340faf
Source noteuspto-grants-2015_08