Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Allyltributylstannane | HCID 90628 | — |
| Reactant | HCID 71657160 | HCID 71657160 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 131736043 | HCID 131736043 | 68% |
Reaction Steps
5-[4-(2-Iodobenzoylamino)phenyl]-1H-naphtho[1,2-b][1,4]diazepine-2,4(3H,5H)-dione (70 mg, 0.128 mmol), allyltributyltin (98 mg, 0.32 mmol), and tetrakistriphenylphosphine palladium(0) (15 mg, 12.8 μmol) were dissolved in anhydrous toluene (0.6 mL), and the solution was stirred at 110° C. for 16 hours. The reaction mixture was left to cool, and then added with acetonitrile, the mixture was washed with petroleum ether, and the solvent of the acetonitrile layer was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform/methanol=100/1) to obtain the title compound (40 mg, yield 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09382236B2 |
|---|
| Source dataset | uspto-grants-2016_07 |
|---|
| ORD ID | ord-0c29225adc2e4596903ac1804c5716ce |
|---|
| Source note | uspto-grants-2016_07 |
|---|