HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-{2-[3-(2-Fluoro-ethoxy)-phenyl]-imidazol[1,2-a]pyrimidin-7-ylcarbamoyl}-1-methyl-1H-pyrazole-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-{2-[3-(2-Fluoro-ethoxy)-phenyl]-imidazo[1,2-a]pyrimidin-7-ylcarbamoyl}-1-methyl-1H-pyrazole-4-carboxylic acid ethyl ester | HCID 53468455 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-{2-[3-(2-Fluoro-ethoxy)-phenyl]-imidazol[1,2-a]pyrimidin-7-ylcarbamoyl}-1-methyl-1H-pyrazole-4-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410117B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-bfe6e50524c945048baf83cbcd03a49b |
| Source note | uspto-grants-2013_04 |