Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 86642943 | HCID 86642943 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 59375012 | HCID 59375012 | — |
Reaction Steps
Step 3 A yellow solution of N-(3-bromo-2-methylphenyl)-2-fluorobenzothioamide (500 mg, 1.542 mmol) in DMSO (5 mL) was treated with anhydrous hydrazine (0.484 mL, 15.42 mmol) and heated at 150° C. After 2 h 20 min the solution was cooled to rt, diluted with NaHCO3 (aq) and extracted twice with EtOAc. The combined organic phases were washed twice with water and once with brine, dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 85:15 to 50:50 hexane-EtOAc) to provide N-(3-bromo-2-methylphenyl)-1H-indazol-3-amine as a tan waxy solid (162 mg, 35%). 1H NMR (400 MHz, chloroform-d) δ 9.38 (1 H, br. s.), 7.49 (1 H, d, J=8.1 Hz), 7.45 (1 H, d, J=7.9 Hz), 7.40 (2 H, d, J=3.5 Hz), 7.19 (1 H, dd, J=7.9, 0.9 Hz), 7.10 (1 H, dt, J=8.1, 4.0 Hz), 6.98 (1 H, t, J=8.1 Hz), 6.10 (1 H, s), 2.49 (3 H, s). Mass spectrum m/z 302, 304 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362065B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-6948a35ce41a4ec588527f1b677a55b6 |
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| Source note | uspto-grants-2013_01 |
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