Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178437648 | HCID 178437648 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 178437650 | HCID 178437650 | — |
Reaction Steps
108 mg (0.27 mmol) cis-3-[7-(4-tert-butylcyclohexyl)-5-ethyl-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl]benzonitrile (Example 40A) are dissolved in concentrated hydrochloric acid, and the reaction mixture is stirred at 95° C. for three hours. Sodium hydroxide (10% aqueous solution) (until a pH of 6–7 is achieved) and ethylacetate are added. The organic phase is dried over sodium sulfate and evaporated to dryness in vacuo. The product is purified by column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07074790B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-8989254712ee4cc1a25f2470b71bdd04 |
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| Source note | uspto-grants-2006_07 |
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