HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibutylxanthine → HCID 11406633, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibutylxanthine | HCID 101421 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11406633 | HCID 11406633 | 51% |
Reaction Steps
A stirred solution of 1,3-di-N-butyl xanthine (100 mg, 3.39 mmol) in anhydrous DMF (3 ml) was treated with NIS (94 mg, 3.75 mmol) and left to stir at rt. under nitrogen for 23 hours. The mixture was partitioned between sat. Na2SO3(aq) solution and EtOAc. The organic layer was separated, washed with brine, dried (MgSO4) and concentrated in vacuo. The product was purified by passing down an SPE (Si, 5 g) cartridge eluting with EtOAc/cyclohexane mixtures. The product fraction was concentrated to afford the title compound as a white solid (75 mg, 51%); NMR; δH (400 MHz, d6-DMSO) (app. td, 6H, J=7.5 and 4 Hz), 1.21-1.34 (m, 4H), 1.45-1.54 (m, 2H), 1.56-1.66 (m, 2H), 3.84 (t, 2H, J=7.5 Hz), 3.93 (t, 2H, J=7.5 Hz), 14.10 (s, 1H); m/z 391.3 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268839B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-f90bfb32739642f693e6405e7ef95123 |
| Source note | uspto-grants-2012_09 |