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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480660Generated: October 30, 2026

Phthalic Anhydride → HCID 178444743, compound

https://huagongshe.com/reaction/480660

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 178444743HCID 17844474349.2%

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 numberUS06653317B2
Source datasetuspto-grants-2003_11
ORD IDord-2a2e345158ae4c349cf2064bc48a3af6
Source noteuspto-grants-2003_11