Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Allyltributylstannane | HCID 90628 | — |
| Reactant | HCID 18466620 | HCID 18466620 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18466626 | HCID 18466626 | 103.2% |
Reaction Steps
Allyltributyltin (98 μL, 0.32 mmol) and Pd(Ph3P)4 (16 mg, 0.02 mmol) were added to a degassed (N2 through solution for 30 min) solution of 8-bromo-5,11-dihydro-11-ethyl-5-methyl-2-(trifluoromethyl)-6H-dipyrido[3,2-b:2′,3′-e] [1,4]diazepin-6-one (11 mg, 0.27 mmol) in DMF (1.4 mL) at room temperature. The mixture was stirred at 90° C. for 1.5 h then was cooled to room temperature and concentrated under reduced pressure. The residue was purified by flash chromatography (hexane:EtOAc, 8:2 to 7:3) to give the title compound (101 mg, 99% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06420359B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-2ca0ad9cda2d442eaad802c72da6e634 |
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| Source note | uspto-grants-2002_07 |
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