Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | HCID 86696284 | HCID 86696284 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86696283 | HCID 86696283 | 13.91% |
Reaction Steps
The solution of (81.1) (256.5 mg, 0.546 mmol) and PdCl2(PPh3)2 (38.4 mg, 0.055 mmol) in DMF (10 ml) was bubbled by N2 for 5 min. Tributyl(1-ethoxyvinyl)stannane (296 mg, 0.820 mmol) was added. The reaction tube was flushed by N2 for 5 min again and sealed. The sealed-tube was stirred at 85° C. for 16 h. The mixture was evaporated to dryness and the residue was purified by flash chromatography (CombiFlash, ISCO, eluent MeOH/DCM from 0 to 10%) to afford the title compound (35 mg, yield 13.91%). LCMS (method A): [M+H]+=461.2, tR=1.96 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062045B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-1f4bcde500564e8eb935b66f3c8eb84f |
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| Source note | uspto-grants-2015_06 |
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