Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 56946380 | HCID 56946380 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 56946484 | HCID 56946484 | — |
Reaction Steps
To a solution of 2-(3,4-dimethoxy-phenylamino)-9-iodo-5H,7H-benzo[b]pyrimido[4,5-d]azepin-6-one (I-30) (100 mg, 0.210 mmol) in 4 mL anhydrous DMF at room temperature was added zinc cyanide (14 mg, 0.120 mmol), tris(dibenzylideneacetone)dipalladium (9.5 mg, 0.01 mmol), 1,1′-bis(diphenyl-phosphino)ferrocene (14.0 mg, 0.02 mmol) and a drop of H2O. The solution was degassed with argon then stirred at 1° C. for 16 h. The solution was allowed to cool to 22° C., then diluted with EtOAc and saturated aqueous sodium bicarbonate. The organic layer was then washed with H2O and brine, dried over Na2SO4, and concentrated in vacuo. The product was recrystallized in methanol and CH2Cl2 to give I-92 (92%): MS Rt═2.49 min, m/z═388 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07459448B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-da1fbb0e418246bfa09aaef98628ae68 |
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| Source note | uspto-grants-2008_12 |
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