HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 11186195, compound → HCID 12097174, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 11186195 | HCID 11186195 | — |
| Reactant | HCID 178506865 | HCID 178506865 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12097174 | HCID 12097174 | — |
Reaction Conditions
| Temperature | -70 °C |
|---|
Reaction Steps
Copper iodide (5 mmol) was suspended in THF (25 ml) under an inert gas atmosphere. The suspension was cooled to −70° C. and n-hexyllithium (5 ml,2M in hexanes) was added by syringe. The mixture was stirred for 45 minutes and 5,7-dichloro-6-(2,4,6-trifluorophenyl)-pyrazolo[1,5-α]pyrimidine (5 mmol, obtained from Example 3) was added as a solution in THF (10 min). The reaction mixture was stirred for 15 minutes at −70° C. The reaction mixture was then quenched with a mixture of aqueous saturated ammonium chloride/concentrated ammonia (9:1). The two phase mixture was separated. An oil was isolated from the organic layer which was subjected to chromatographic purification which yields the product as a crystalline residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06552026B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-a46fef191bc642cc9aed03472d87027e |
| Source note | uspto-grants-2003_04 |