Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Aminoindole | HCID 78867 | — |
| Reactant | 6-[2-(4-Pyridinyl)ethenyl]-4(3H)-quinazolinone | HCID 136038668 | — |
| Product | HCID 70241132 | HCID 70241132 | 74.3% |
Reaction Steps
The title compound (250 mg, 1.0 mmol) from Example 20 was activated in an analogous method to Example 21 and combined with 5 -aminoindole (171 mg, 1.3 mmol). The reaction mixture was heated at 60° C. overnight and then cooled to room temperature. The resin was filtered off and the solution was concentrated in vacuo. The crude residue was chromatographed on silica gel in 10% acetone/ethyl acetate to provide 270 mg (74%) of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06225318B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-2b3dc3c24c4a44a59607eea7b495a385 |
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| Source note | uspto-grants-2001_05 |
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