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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238413Generated: October 28, 2026

HCID 67176053, compound → HCID 46179476, compound

https://huagongshe.com/reaction/238413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67176053HCID 67176053—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 46179476HCID 4617947651%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642628B2
Source datasetuspto-grants-2014_02
ORD IDord-aa3c92f53b844ab683251691d07618d7
Source noteuspto-grants-2014_02