Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | 4-(Trifluoromethoxy)aniline | HCID 600848 | — |
| Reactant | 2,6-dichloro-9-(tetrahydro-3-thienyl)-9H-purine | HCID 21922991 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 21922986 | HCID 21922986 | — |
Reaction Steps
The operation is carried out as in Stage 2 of Example 5 starting from 160 mg of the product obtained in Stage 1 of Example 5, 3 ml of butanol and using 0.081 ml of 4-(trifluoro-methoxy)-benzenamine in place of the benzylamine and the reaction medium is taken to a temperature of approximately 80 to 85° C. for approximately 20 hours, left to return to ambient temperature, diluted with 3 ml of isopropanol, placed for approximately one hour at a temperature of approximately 0° C., followed by separating, washing with 5 ml of isopropanol and drying under vacuum at a temperature of approximately 50° C. After purification on silica eluting with methylene chloride/ethyl acetate in a proportion of 90/10, 203 mg of expected product is obtained in the form of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07122669B1 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-bf76959bf13a41c9beb4ebc805dff15b |
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| Source note | uspto-grants-2006_10 |
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