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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200921Generated: October 28, 2026

Phthalic Anhydride → HCID 136133144, compound

https://huagongshe.com/reaction/2200921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantTriethylamineHCID 8471—
ReactantHCID 136133146HCID 136133146—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
ProductHCID 136133144HCID 136133144—

Reaction Steps

Under argon, ethyl 2-amino-7-(4-cyanophenyl)-5-methyl-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate (5.0 g, 15.4 mmol) and phthalic anhydride (3.4 g, 23.1 mmol, 1.5 eq.) were dissolved in a mixture of toluene (400 ml) and pyridine (200 ml), triethylamine (42 μl, 0.3 mmol, 0.2 eq.) was added and the mixture was heated under reflux for 12 h. The reaction mixture was then concentrated under reduced pressure. The residue was taken up in ethyl acetate (600 ml) and extracted twice with saturated sodium bicarbonate solution (150 ml each). The organic phase was washed with saturated sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure. The crude product was suspended in ethanol (100 ml) and stirred for 12 h, and the solid was then filtered off and dried under high vacuum. This gave 6.67 g (95% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359362B2
Source datasetuspto-grants-2016_06
ORD IDord-e8c4a6bee8934126854ce92c79c54ac4
Source noteuspto-grants-2016_06