Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 6-chloro-2-(trifluoromethyl)-7H-purine | HCID 6053911 | — |
| Reactant | HCID 178455851 | HCID 178455851 | — |
| Catalyst | HCID 178418745 | HCID 178418745 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69081211 | HCID 69081211 | 30% |
Reaction Steps
1-Propyl magnesium bromide (3.0 mmol) was added to a mixture of 6-chloro-2-trifluoromethylpurine 222 mg (1.0 mmol), [1,3-bis(diphenylphosphino)-propane]dichloronickel(II) (0.04 mmol) and THF 15 ml at 20° C. under nitrogen. The reaction mixture was allowed to stirred at 50° C. for 12 hours, then cooled to 20 ° C., and 0.2 ml of water was added to quench the reaction. The mixture was diluted with 20 ml ethyl acetate and filtered over celite. Evaporation under vacuo and chromatography (MeOH:EtOAc:hexane=2:50:50) gave the title compound with 30% yield. 1H NMR (300 MHz, CDCl3) δ 8.10 (s, 1H), 7.27 (t, J=8.37 Hz, 1H), 3.29 (t, J=7.5 Hz, 2H), 1.95 (m,2H), 1.02 (t, 7.5 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07335654B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-df4416aaae82483e8950c83cbcb1627c |
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| Source note | uspto-grants-2008_02 |
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