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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092033Generated: October 30, 2026

Ammonia → HCID 59574209, compound

https://huagongshe.com/reaction/2092033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTrifluoroacetic acidHCID 6422—
Reactant3,6-DichloropyridazineHCID 67331—
Reactant2-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)butanoic acidHCID 344256—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 59574209HCID 59574209—

Reaction Steps

3,6-Dichloropyridazine (596 mg, 4 mmol), 2-(1,3-dioxoisoindolin-2-yl)butanoic acid (1.59 g, 6.8 mmol), silver nitrate (67.9 mg, 0.4 mmol), trifluoroacetic acid (91.2 mg, 0.8 mmol) and water (10 mL) were heated at 70° C. with stirring, and to the resulting mixture, diammonium peroxodisulfate (1.64 g, 7.2 mmol) in water (2 mL) was added dropwise over 30 minutes. After the dropwise addition, the resulting reaction mixture was stirred at 70° C. for 30 minutes, then mixed with 10 mL of ethyl acetate and allowed to cool to room temperature. The reaction mixture was cooled with ice, then basified with 28% aqueous ammonia (to pH 9) and extracted with ethyl acetate. The resulting organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (chloroform/ethyl acetate=1/1) to give a crude product, which was used for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440666B2
Source datasetuspto-grants-2013_05
ORD IDord-2514f879782a4a9da329e78f392b9efc
Source noteuspto-grants-2013_05