HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238413Generated: October 28, 2026
HCID 67176053, compound → HCID 46179476, compound
https://huagongshe.com/reaction/238413
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67176053 | HCID 67176053 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 46179476 | HCID 46179476 | 51% |
Reaction Steps
A mixture of ethyl 3-(1-(4-(1H-imidazol-1-yl)phenyl)-2-(4-carbamoyl-2-methylphenyl)-1H-pyrrol-3-yl)propanoate (25 mg, 0.057 mmol) and LiOH monohydrate (42 mg, 1 mmol) in a mixture of methanol (1.5 mL) and water (0.5 mL), and the reaction mixture was stirred at room temperature overnight. Methanol was removed under reduced pressure, and the residue was diluted with water (5 mL), and the aqueous layer was washed with ethyl acetate (5 mL×3). The aqueous layer was adjusted to PH=6˜7 with 1N HCl, and the resulting mixture was extracted with a mixture of dichloromethane and isopropanol (3:1, 5 mL×3). The combined organic layer was dried, and evaporated to give 3-(1-(4-(1H-imidazol-1-yl)phenyl)-2-(4-carbamoyl-2-methylphenyl)-1H-pyrrol-3-yl)propanoic acid, (5-4, R1=1H-imidazol-1-yl) (12 mg, yield: 51%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642628B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-aa3c92f53b844ab683251691d07618d7 |
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| Source note | uspto-grants-2014_02 |
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