Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | 1H-Indazol-6-amine | HCID 81423 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-hydroxy-1H-indazole | HCID 135483987 | — |
Reaction Steps
Indazol-6-amine (24.33 g; manufactured by Tokyo Chemical Industry, Co., Ltd.) was dissolved in water (100 mL) and 48% by weight of tetrafluoroboric acid solution (242 mL; manufactured by Sigma-Aldrich Co.). After cooling to 0° C., an aqueous solution of sodium nitrite [20 mL (sodium nitrite (13.87 g; manufactured by Kanto Chemical Co., Inc.) was dissolved in water (20 mL) to give the solution] was added dropwise thereto for 10 minutes, followed by stirring at 0° C. for 30 minutes. The precipitate from the reaction solution was filtered and washed with chloroform. Thus-obtained precipitate was dissolved in acetic acid (250 mL) and stirred for 10 minutes at 50° C., 10 minutes at 110° C., and 10 minutes at 130° C. The reaction solution was cooled and added with a saturated aqueous solution of sodium carbonate, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and then dried. Thereafter, the solvent was evaporated under reduced pressure. Thus-obtained residue was dissolved in ethanol (240 mL), added with an aqueous solution of 2 mol/L-sodium hydroxide (365 mL), followed by stirring at room temperature for 1 hour. The reaction solution was concentrated under reduced pressure, and 2 mol/L-hydrochloric acid (200 mL), water and a saturated aqueous solution of ammonium chloride were added to the residue to obtain pH 7 approximately, and the extraction was carried out with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. To the residue, chloroform was added, and then the insoluble matters were filtered, washed with chloroform to obtain the target compound as a crude product (13.5401 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304443B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-c580faf72b7e4ca68c6dfe35d01afea6 |
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| Source note | uspto-grants-2012_11 |
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