HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394723Generated: October 29, 2026
Maleic Anhydride → HCID 54170922, compound
https://huagongshe.com/reaction/394723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | 7-Amino-4-[(3-bromophenyl)amino]quinazoline | HCID 5328045 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54170922 | HCID 54170922 | 17.4% |
Reaction Steps
To a 50° C. solution of 0.158 g of 7-amino-4-(3-bromoanilino)-quinazoline (J Med Chem, 1995:3482) in 10 mL of tetrahydrofuran was added 0.059 g of maleic anhydride. The cold solution stirred for 15 minutes, and then the ice bath was removed. The reaction warmed to room temperature where it continued stirring for 15 hours. The suspension was heated under reflux for 30 minutes and then stirred at room temperature another 15 hours. Another 0.059 g of maleic anhydride and 20 mL of tetrahydrofuran were added, and the reaction was refluxed for an additional 2 hours. After another 15 hours at room temperature, the reaction was refluxed for 15 hours. The reaction was filtered, and the light tan solid was recrystallized first from dimethyl-formamide and then a second time from methanol to afford 0.036 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06602863B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-a7dca76a54a848ab88be31fd141e30bd |
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| Source note | uspto-grants-2003_08 |
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