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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911076Generated: October 30, 2026

Propanedioic acid, monoethyl ester → HCID 86634786, compound

https://huagongshe.com/reaction/911076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanedioic acid, monoethyl esterHCID 3595298—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
ReactantHCID 86634782HCID 86634782—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86634786HCID 8663478650.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A flask was charged with 2-(5-bromo-2-(4-phenethylthiazol-2-ylamino)pyridin-4-yl)acetic acid (0.576 g, 1.377 mmol) and THF (20 mL), and carbonyl diimidazole (0.3014 g, 1.859 mmol) was added. The mixture was heated at 50° C. for 2 hours. In a separate 50 mL scintillation vial, mono-ethyl malonate (0.2845 ml, 2.410 mmol) was dissolved in THF (15 mL) and cooled to 0° C., and isopropyl magnesium chloride (2.410 mL, 4.819 mmol) was added. This second mixture was stirred at ambient temperature for 30 minutes, then heated to 50° C. and stirred another 30 minutes. Both solutions were cooled to 0° C. and the second mixture was added to the first mixture. The combined mixture was stirred at ambient temperature overnight, then quenched with saturated ammonium chloride solution and extracted with ethyl acetate. The combined extracts were washed with water and brine, dried and evaporated. The residue was purified by silica gel chromatography, eluting with 20% ethyl acetate/hexane to provide the desired product (0.337 g, 46-10% yield) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022222B2
Source datasetuspto-grants-2011_09
ORD IDord-92ac2a32e06b4e2597398ce69a8edc6a
Source noteuspto-grants-2011_09