Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-(Triisopropylsilyl)pyrrole-3-boronic acid | HCID 2763303 | — |
| Reactant | HCID 178480720 | HCID 178480720 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178480727 | HCID 178480727 | 31.2% |
Reaction Steps
To a suspension of 6-bromo-4-{[4-(4-methyl-piperazin-1-yl)-phenylamino]-methylene}-4H-isoquinoline-1,3-dione (0.2 g, 0.45 mmol) in N,N-dimethylformamide (5 mL) is added N-triisopropylsilyl-3-pyrrole boronic acid (0.16 g, 0.54 mmol), followed by 300 μL of 2M aqueous cesium carbonate and tetrakis triphenylphosphine palladium (30 mg, 0.025 mmol). The reaction mixture is subjected to microwave heating at 180° C. for 300 seconds. The reaction mixture is then divided into 3 fractions and purified by C18 reverse phase HPLC. The pure fractions were combined and concentrated to yield 60 mg of 4-{[4-(4-methyl-piperazin-1-yl)-phenylamino]-methylene}-6-(1H-pyrrol-3-yl)-4H-isoquinoline-1,3-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713994B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-615acb04e45843bb98edc0a0020b8374 |
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| Source note | uspto-grants-2010_05 |
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