HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoylhydrazine → HCID 86587505, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Reactant | HCID 86587503 | HCID 86587503 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 86587505 | HCID 86587505 | — |
Reaction Steps
Toluene-4-sulfonic acid 5acetyl-4-(2-fluorophenyl)-1H-pyrazol-3-yl ester (1.0 g, 2.7 mmol; prepared as described in Example 1, steps a to c) was stirred with benzhydrazide (400 mg, 2.9 mmol) in xylene (30 ml) at reflux overnight. The mixture was allowed to cool to room temperature. A solid crystallised out of solution This was separated by filtration, and was recrystallised from ethyl acetate, yielding toluene-4-sulfonic acid 3-(2-fluorophenyl)-4-methyl-7-phenylpyrazolo[1,5-d][1,2,4]triazin-2-yl ester as a white solid (694 mg). 1H NMR (400 MHz, CDCl3) δ 2.47 (3H, s), 2.52 (3H, s), 7.19 (1H, t, J=8.9 Hz), 7.28 (3H, m), 7.41-7.52 (4H, m), 7.61 (1H, m), 7.79 (2H, d, J=8.3 Hz), 8.25 (2H, d, J=7.5 Hz); MS (ES+) m/e 475 [MH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06872720B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-95c1bdba5e1e469a967d81a2526f8c44 |
| Source note | uspto-grants-2005_03 |