Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-Indazole | HCID 9221 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Iodo-4H-chromen-4-one | HCID 10901720 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54413098 | HCID 54413098 | 88.5% |
Reaction Steps
To an eggplant type flask (25 ml), 3-iodochromone (136 mg) prepared in Example 1, indazole (236 mg), potassium carbonate (1382 mg), and dimethylformamide (15 mg) were added and the mixture was reacted at 80° C. for 30 hours with stirring. The reaction mixture was added to ice water and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purifiedby the silica gel column chromatography, and the purified product was recrystallized from benzene/hexane to give the titled compound (113.6 mg; yield=88.5%) as crystals. Melting point: 237°-238° C. 1H-NMR(CDCl3, δ ppm): 6.94 (s, H3), 8.26 (dd, H5), 7.58-7.68 (m, H6), 7.75 (t, H7), 7.58-7.68 (m, H8), 8.30 (s, H3'), 7.82 (m, H4'), 7.35-7.53 (m, H5'), 7.35-7.53 (m, H6'), 8.26 (m, H7') .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05698575 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-cb22f5da32ab4e8e817ca5cda0b0e551 |
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| Source note | uspto-grants-1997_12 |
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