HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868095Generated: October 29, 2026
Potassium Cyanide → HCID 14280881, compound
https://huagongshe.com/reaction/868095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 54234399 | HCID 54234399 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14280881 | HCID 14280881 | 10.2% |
Reaction Steps
To a suspension of 2.78 g (10 mmole) of 7-amino-1,4-dihydro-1-ethyl-6-fluoro-3-quinolinecarboxylic acid ethyl ester in 40 ml of 1N HCl at 8° was added a solution of 0.72 g (10.5 mml) of sodium nitrite and 5 ml of water portionwise keeping the temperature at 8° C. The orange solution was stirred at 5° to 8° C. for 0.5 hours. To a solution of 1.07 g (12 mmol) of cuprous cyanide, 2.28 g (35 mmol) of potassium cyanide and 25 ml of water at 45°-50° C. was added the diazonium solution over 10 minutes. The foaming mixture was heated with stirring at 50°-60° C. for 1.25 hours, then treated with 10 ml of 29% ammonium hydroxide and stirred at 50° C. for 20 minutes. The solution was cooled with ice and the solid collected by filtration. The solid was recrystallized from acetonitrile to give 0.28 g of the title compound, mp 205°-207° C. The acetonitrile filtrate was evaporated to dryness and the residue was triturated with ethers to yield an additional 0.63 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04777175 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-28983e94af404b37afd34ec5662c3cc6 |
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| Source note | uspto-grants-1988_10 |
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