Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Reactant | HCID 178439173 | HCID 178439173 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178439174 | HCID 178439174 | — |
Reaction Steps
1.8 g (4.24 mM) of ethyl 5-[4-carbamoyl-5-(4-propylbenzoylamino)-1H-imidazol-2-ylmethyl]furan-2-carboxylate are added to 10 ml of an ethanol/THF mixture (50-50). 4 ml of aqueous 3N sodium hydroxide solution are then added and the reaction medium is maintained at 40° C. with stirring for 2 hours. The reaction medium is allowed to cool and is acidified with acetic acid; a solid crystallizes. The solid is filtered off and washed with demineralized water to give, after drying, 1.7 g of 5-[4-carbamoyl-5-(4-propylbenzoylamino)-1H-imidazol-2-ylmethyl]furan-2-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362057B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-6c36c6e0d69c4f6aa4173c0dbf6c59a1 |
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| Source note | uspto-grants-2013_01 |
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