HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397362Generated: October 28, 2026
1H-Pyrazol-3-amine, 5-methyl- → HCID 178428185, compound
https://huagongshe.com/reaction/397362
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-Pyrazol-3-amine, 5-methyl- | HCID 93146 | — |
| Reactant | 4-chloro-2-phenylquinoline | HCID 278376 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | HCID 178428185 | HCID 178428185 | — |
Reaction Steps
To a mixture of 4-chloro-2-phenylquinoline (J. Het. Chem., 20, 1983, 121-128)(0.53 g, 2.21 mmol) in diphenylether (5 mL) was added 3-amino-5-methylpyrazole (0.43 g, 4.42 mmol) and the resulting mixture heated at 200° C. overnight with stirring. The reaction mixture was cooled to ambient temperature then petroleum ether (20 mL) was added and the resulting precipitate was isolated by filtration. The crude solid was purified by flash chromatography (SiO2, gradient DCM-MeOH) to afford V-4 as a white solid: mp 242-244° C.; 1H NMR (DMSO) δ2.27(3H, s), 6.02(1H, s), 7.47(2H, d), 7.53-7.40(2H, br m), 7.67(1H, m), 7.92(1H, m), 8.09(2H, d), 8.48(2H, m), 9.20(1H, s), 12.17(1H, br s); IR (solid) 1584, 1559, 1554, 1483, 1447, 1430, 1389; MS 301.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610677B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-addfcf6671dc451a95d4c45f1c62c78a |
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| Source note | uspto-grants-2003_08 |
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