HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3-Chlorophenyl)hydrazine → HCID 178419962, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3-Chlorophenyl)hydrazine | HCID 75332 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 68153171 | HCID 68153171 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178419962 | HCID 178419962 | 10.6% |
Reaction Steps
To a solution of 0.1 g (0.2579 mmol) (Z)-3-(2-chloro-6-fluorophenyl)-5-(1-(dimethylamino)-4,4,4-trifluoro-3-oxobut-1-en-2-yl)isoxazole-4-carbonitrile in dry ethanol, 0.0462 g (0.2579 mmol) 3-Chlorophenylhydrazine and 0.78 mL (0.2579 mmol) DIPEA were added. The reaction mixture was heated under reflux for 3 h. The mixture was concentrated in vacuo and was dried in high vacuum. Purification was achieved by using pTLC, and 0.0037 g (yield of theory: 3.0%) of the pyrazolyl-isoxazole derivativewere obtained. Result of LC/MS MH+: 466.9; 1H NMR (DMSO-d6; CCl4): 7.73-7.97 (6H, m, CH-arom.), 8.04 (1H, s, CH-arom.), 8.81 (1H, s, CH-pyraz.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354436B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-e460095a74fd49a9926dbb9a209d5b6c |
| Source note | uspto-grants-2013_01 |