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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958359Generated: October 31, 2026

Hydrochloric Acid → 5-{2-[3-(2-Fluoro-ethoxy)-phenyl]-imidazol[1,2-a]pyrimidin-7-ylcarbamoyl}-1-methyl-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1958359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
Reactant5-{2-[3-(2-Fluoro-ethoxy)-phenyl]-imidazo[1,2-a]pyrimidin-7-ylcarbamoyl}-1-methyl-1H-pyrazole-4-carboxylic acid ethyl esterHCID 53468455—
SolventWaterHCID 962—
Product5-{2-[3-(2-Fluoro-ethoxy)-phenyl]-imidazol[1,2-a]pyrimidin-7-ylcarbamoyl}-1-methyl-1H-pyrazole-4-carboxylic acidHCID 53468646—

Reaction Steps

Ethyl 5-(2-(3-(2-fluoro ethoxy)phenyl)imidazo[1,2-a]pyrimidin-7-ylcarbamoyl)-1-methyl-1H-pyrazole-4-carboxylate (100 mg, 221 μmol) was combined with Ethanol (0.570 ml) and THF (0.570) to give a yellow solution. The reaction was stirred at RT for 6 h. H2O was added to the suspension and then HCl 1N was added until the mixture was acidic (pH=3). The suspension was stirred for 30 min and then the reaction mixture was filtered. The residual solvent was removed under vacuum. The title compound was obtained as a light yellow solid (73 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410117B2
Source datasetuspto-grants-2013_04
ORD IDord-bfe6e50524c945048baf83cbcd03a49b
Source noteuspto-grants-2013_04