Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 2,2-Diphenylethylamine | HCID 77575 | — |
| Reactant | 2,6-Dichloropurine | HCID 5324412 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178478404 | HCID 178478404 | — |
Reaction Steps
2,6-Dichloropurine (20.00 g, 106 mmol) is dissolved in THF (250 ml) under an atmosphere of argon. Diisopropylamine (16.38 g, 127 mmol) is added followed by 2,2-diphenylethylamine (25.00 g, 127 mmol) and the reaction mixture is stirred at 50° C. The reaction is shown to be complete by LCMS after 6 hours. 50% of the solvent is removed in vacuo and replaced with MeOH. The resulting precipitate is filtered off and dried to give the title compound. 1H nmr (d6-DMSO, 400 MHz); 8.05(br s, 1H), 7.35-7.10(m, 10H), 4.55(m, 1H), 4.10(rri, 2H), MS (ES+) m/e 350 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163754B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-ac9fd4f751534004a806e085e5818a7b |
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| Source note | uspto-grants-2012_04 |
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