Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Reactant | 2,6-Dichloropurine | HCID 5324412 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Solvent | 1-Pentanol | HCID 6276 | — |
| Product | 190654-89-8 | HCID 21988300 | — |
Reaction Steps
To a suspension of 2,6-dichloropurine (3.78 g; 0.02 mol) and m-anisidine (3.69 g; 0.03 mol) in n-pentanol (40 ml), triethylamine (7 ml; 0.05 mol) was added. The reaction mixture was stirred at 100° C. for 4 hours and then it was allowed to cool to the room temperature. The white precipitate was collected, washed with isopropanol (2×10 ml) and water (3×10 ml). The crude product was purified by the crystallization from methanol in the presence of activated charcoal to give white crystals. Yield: 4.36 g (77.8%). TLC (chloroform-methanol; 85:15): one single spot, free of starting material, HPLC purity: 98+%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222260B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-be0f744ada424c1dafc63343e9edfeeb |
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| Source note | uspto-grants-2012_07 |
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