HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805259Generated: November 1, 2026
(3-Chlorophenyl)hydrazine → HCID 178419962, compound
https://huagongshe.com/reaction/1805259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (3-Chlorophenyl)hydrazine | HCID 75332 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 3730890 | HCID 3730890 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178419962 | HCID 178419962 | 225.8% |
Reaction Steps
To a solution of 0.5047 g (1.1994 mmol) methyl 3-(2-chloro-6-fluorophenyl)-5-(1-(dimethylamino)-4,4,4-trifluoro-3-oxobut-1-en-2-yl)isoxazole-4-carboxylate in dry ethanol, 0.1790 g (0.9995 mmol) 3-Chlorophenylhydrazine and 0.17 mL (0.9995 mmol) N,N-Diisopropylethylamine (DIPEA) were added. The reaction mixture was heated under reflux for 2 h. The product was isolated by using column chromatography (Petroleum ether:Diethyl ether 80:20), and 0.305 g (yield of theory: 61%) of the pyrazolyl-isoxazole derivative were obtained. Result of LC/MS [M+H]+: 499.9; 1H NMR (DMSO-d6; CCl4): 3.66 (3H, s, CH3), 7.45-7.50 (1H, dd, CH-arom.), 7.55-7.58 (1H, d, CH-arom.), 7.65-7.77 (1H, d, CH-arom.), 7.65-7.77 (1H, dd, CH-arom. phenylhydrazine), 7.65-7.77 (1H, d, CH-arom. phenylhydrazine), 7.85 (1H, s, CH-arom phenylhydrazine), 8.56 (1H, s, 1-pyrazole)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08354436B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-ef8eb5c93d674f01a8aa54cf900f98ef |
|---|
| Source note | uspto-grants-2013_01 |
|---|