HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 3-{1-[3-(5-Methylpyrimidin-2-yl)benzyl]-6-oxo-1,6-dihydropyridazin-3-yl}benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-(6-Oxo-1,6-dihydropyridazin-3-yl)benzonitrile | HCID 20326520 | — |
| Reactant | Diisopropyl diazodicarboxylate | HCID 22145704 | — |
| Reactant | [3-(5-Methylpyrimidin-2-yl)phenyl]methanol | HCID 59484945 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-{1-[3-(5-Methylpyrimidin-2-yl)benzyl]-6-oxo-1,6-dihydropyridazin-3-yl}benzonitrile | HCID 59484891 | — |
Reaction Steps
8.3 147 μl (0.75 mmol) of diisopropyl diazodicarboxylate are added dropwise to a suspension of 98.6 mg (0.50 mmol) of 3-(6-oxo-1,6-dihydropyridazin-3-yl)benzonitrile, 100 mg (0.50 mmol) of [3-(5-methylpyrimidin-2-yl)phenyl]methanol and 197 mg (0.75 mmol) of triphenylphosphine in 3 ml of THF, and the resultant solution is stirred at room temperature for 18 hours. The reaction mixture is evaporated in vacuo, and 2-propanol is added to the residue. The resultant precipitate is filtered off with suction and chromatographed on a silica gel column with dichloromethane/methanol as eluent: 3-{1-[3-(5-methylpyrimidin-2-yl)benzyl]-6-oxo-1,6-dihydropyridazin-3-yl}benzonitrile (“A15”) as yellowish solid; ESI 380;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921357B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-0258cf21d3de434b872b5784d05811f8 |
| Source note | uspto-grants-2014_12 |