HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480660Generated: October 30, 2026
Phthalic Anhydride → HCID 178444743, compound
https://huagongshe.com/reaction/480660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Chloro-N4-hexyl-2,4-pyrimidinediamine | HCID 11183788 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 178444743 | HCID 178444743 | 49.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06653317B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-2a2e345158ae4c349cf2064bc48a3af6 |
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| Source note | uspto-grants-2003_11 |
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