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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572260Generated: October 31, 2026

HCID 67176053, compound → HCID 46179476, compound

https://huagongshe.com/reaction/572260

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 numberUS09029402B2
Source datasetuspto-grants-2015_05
ORD IDord-c99e5f532ee54d4f83e8dbddd6a2f2b8
Source noteuspto-grants-2015_05