Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 1-(5-Bromo-2-fluorophenyl)butan-1-one | HCID 52983815 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178440402 | HCID 178440402 | 52.3% |
Reaction Steps
To 1-(5-bromo-2-fluorophenyl)butan-1-one (2.0 g, 8.1 mmol) in THF, anhydrous hydrazine (11 mL) in THF was added and heated at reflux (60-70° C.) for 5-6 hours. Xylene was added to the reaction mixture and heated at reflux for 20-24 hours. The reaction mixture was concentrated to give a crude product, which was purified by column chromatography using 15% ethyl acetate/pet-ether as eluents to afford 5-bromo-3-propyl-1H-indazole (1.02 g, 52.3%) as a solid. 1H NMR (CDCl3): δ 7.9 (s, 1H), 7.4 (d, 1H), 7.3 (d, 1H), 2.9 (t, 2H), 1.8 (q, 2H), 1.0 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318762B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-60eceb282a984d9fb3824e3c9025c7d3 |
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| Source note | uspto-grants-2012_11 |
|---|