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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635766Generated: November 2, 2026

Phthalic Anhydride → HCID 178444740, compound

https://huagongshe.com/reaction/1635766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantSodium HydroxideHCID 14798—
Reactant6-Chloro-N4-hexyl-2,4-pyrimidinediamineHCID 11183788—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventDiisopropyl EtherHCID 7914—
ProductHCID 178444740HCID 17844474042.2%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

5.95 g of urea/H2O2 complex and 9.07 g of phthalic anhydride were suspended in 90 ml of isopropanol, in a three-necked flask. The mixture was stirred for 30 min at room temperature (20-25° C.). 10 g of 2-amino-4-hexylamino-6-chloropyrimidine were then added while controlling the exotherm at +30° C. After reaction for 3 hours, 100 ml of sodium hydrogen sulfite were poured thereinin to destroy the residual oxidizing agents. The mixture was permitted to separate out by settling and the upper phase was concentrated under vacuum. The residue obtained was taken up in a water (80 ml)/30% sodium hydroxide (20 ml) mixture. The solid obtained was reimpasted in 150 ml of isopropyl ether. The solid was filtered off and washed. It was dried in a heated desiccator. 4.52 g of the expected compound were thus obtained, for a yield of 42%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511659B2
Source datasetuspto-grants-2003_01
ORD IDord-a56f5114d8044557b618d21df28f6115
Source noteuspto-grants-2003_01