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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433481Generated: October 30, 2026

Acetic Anhydride → HCID 22936416, compound

https://huagongshe.com/reaction/1433481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSuccinic anhydrideHCID 7922—
ReactantSodium AcetateHCID 517045—
ReactantN1-cyclopropyl-5-((2-amino-4-pyridyl)oxy)-1H-1-indolecarboxamideHCID 21949236—
SolventTolueneHCID 1140—
ProductHCID 22936416HCID 22936416—

Reaction Conditions

Temperature80 °C

Reaction Steps

N1-Cyclopropyl-5-[(2-amino-4-pyridyl)oxy]-1H-1-indolecarboxamide (830 mg), succinic anhydride (270 mg) and toluene (30 ml) were refluxed together for 30 minutes. After adding 50 ml of acetic anhydride and 82 mg of sodium acetate to the reaction solution, the mixture was stirred at 80° C. for 15 minutes. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate). The second eluted substance was N1-cyclopropyl-5-{[2-(2,5-dioxotetrahydro-1H-1-pyrrolyl)-4-pyridyl]oxy}-1H-1-indolecarboxamide, of which 440 mg was obtained as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-02586d11f8874a148c97851a501dcabf
Source noteuspto-grants-2009_11