HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34629Generated: October 27, 2026
Sodium Cyanide → 4-Hydroxyquinazoline-6-carbonitrile
https://huagongshe.com/reaction/34629
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 6-Amino-3,4-dihydroquinazolin-4-one | HCID 135478037 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Hydroxyquinazoline-6-carbonitrile | HCID 135703883 | 26% |
Reaction Steps
6-Aminoquinazolin-4(3H)-one was slurried in 300 ml of 5% hydrochloric acid and the reaction mixture was cooled to 5° C. A solution of 6.72 g (0.097 mol) of sodium nitrite in 30 ml of water was added dropwise over 2.5 hours while maintaining the reaction temperature below 10° C. The resulting diazonium salt was then added portionwise to a hot (86° C.) solution of 7.84 g (0.0876 mol) of copper cyanide and 11.0 g (0.224 mol) sodium cyanide in 60 ml of water. Evolution of nitrogen was evident throughout the addition. After stirring for 30 minutes, the reaction mixture was filtered, washed with water, and air-dried. The crude product (9.1 g) was purified by silica gel chromatography to afford 3.89 g (26%) of the title compound; m.p. 294°-300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04762838 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-cf901b7347db4b2fa3ec85c21e10a335 |
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| Source note | uspto-grants-1988_08 |
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