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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821353Generated: October 31, 2026

Phthalic Anhydride → (E)-2-{2-[2-(1H-indazol-3-yl)vinyl]phenyl}isoindole-1,3-dione

https://huagongshe.com/reaction/1821353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantTriethylamineHCID 8471—
ReactantHCID 69001756HCID 69001756—
SolventO-XyleneHCID 7237—
Product(E)-2-{2-[2-(1H-indazol-3-yl)vinyl]phenyl}isoindole-1,3-dioneHCID 690044954.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

Compound 2 (0.06 g, 0.25 mmol) was dissolved in xylene (2.0 mL) and the solution was added with phthalic anhydride (83 mg, 0.56 mmol) and triethylamine (89 μL, 0.64 mmol), followed by stirring at 60° C. for 2 hours. Then, the reaction mixture was extracted with ethyl acetate. The organic layer was sequentially washed with water and saturated brine, dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The residue was triturated in ethanol to obtain Compound 159 (4.0 mg, 4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605272B2
Source datasetuspto-grants-2009_10
ORD IDord-1878ffb68d2d46f69a3d01ba442c1386
Source noteuspto-grants-2009_10