HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 1H-Purine, 6-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 6-Chloropurine | HCID 5359277 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Catalyst | HCID 178420554 | HCID 178420554 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1H-Purine, 6-methyl- | HCID 5287547 | — |
Reaction Steps
A suspension of 6-chloropurine (0.2 mmol) and tetrakis(triphenylphosphino)-palladium (0.02 mmol) in dry THF (3 mL) was treated with trimethylaluminum (2M in toluene, 0.45 mmol) under nitrogen. The resulting solution was heated to reflux for 3 h, cooled to r.t., diluted with toluene (5 mL), and quenched with methanol (0.5 mL) followed by ammonium chloride (1 mmol). The mixture was heated to reflux for 2 h and filtered while hot through a Celite plug. Evaporation and purification by prep TLC afforded the 6-methylpurine. See J. Med. Chem. 1999, 42, 2064–2086.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138401B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-cc665f81c1814c16ac745e8c85bdae31 |
| Source note | uspto-grants-2006_11 |