HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051119Generated: November 3, 2026
Ethanol → 7-ethoxy-N-(3-ethynylphenyl)-6-nitroquinazolin-4-amine
https://huagongshe.com/reaction/1051119
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | N-(3-ethynylphenyl)-7-fluoro-6-nitroquinazolin-4-amine | HCID 59142759 | — |
| Product | 7-ethoxy-N-(3-ethynylphenyl)-6-nitroquinazolin-4-amine | HCID 86730376 | 93.4% |
Reaction Steps
Na (1.4 g, 0.060 mol) was carefully dissolved in 80 ml of anhydrous ethanol to form a clear solution, then N-(3-ethynylphenyl)-7-fluoro-6-nitroquinazolin-4-amine (8 g, 0.025 mol) was added and stirred for 4 hours at 80° C. The solution was concentrated under reduced pressure to remove excess ethanol, and 50 ml H2O was added. The resulting solid precipitate was filtered and dried under vacuum to get 7-ethoxy-N-(3-ethynylphenyl)-6-nitroquinazolin-4-amine as yellow solid 8.1 g (93.4% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388160B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-ceb948152e1444e1b1337ab358f0337b |
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| Source note | uspto-grants-2016_07 |
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