HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067485Generated: October 31, 2026
Formamidine acetate → HCID 10131272, compound
https://huagongshe.com/reaction/1067485
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | 2-fluoro-6-(4-fluorophenoxy)benzonitrile | HCID 2737320 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 10131272 | HCID 10131272 | 10.7% |
Reaction Steps
A mixture of 2-fluoro-6-(4-fluorophenoxy)benzonitrile (2.5 g, 11 mmol) and formamidine acetate (Aldrich) (2.3 g, 22 mmol) in 50 ml of N,N-dimethylacetamide was heated at 162° C. under nitrogen for 9 hours. After cooling to room temperature the reaction mixture was evaporated under reduced pressure. The product was suspended in 80 ml of cold water and the pH adjusted to 8.5 with concentrated ammonium hydroxide. After cooling the suspension overnight, the precipitate was isolated by filtration, washed with water (25 ml), dried and recrystallized from 30 ml of ethanol at 4° C. The precipitate was collected by filtration, washed with ethanol and dried at 50° C. in vacuo to give 4-amino-5-(4-fluorophenoxy)quinazoline (0.3 g, 10.7%, m.p. 188-190° C.):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248771B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-c7fdb2520f084736b3bd454d73a88615 |
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| Source note | uspto-grants-2001_06 |
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