HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → HCID 178433617, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | 3-Quinolinecarboxylic acid, 4-chloro-2-methyl-, ethyl ester | HCID 10538604 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178433617 | HCID 178433617 | — |
Reaction Steps
The mixture of 3.6 g of ethyl 4-chloro-2-methylquinolin-3-carboxylate, 1.8 g of phenylhydrazine and 40 ml of xylene is refluxed for 4 hours, cooled to room temperature, diluted with diethyl ether and filtered. The residue is dissolved in 50 ml of 2 N aqueous sodium hydroxide, the solution washed with diethyl ether and its pH adjusted to 8.5 with ammonium chloride. The precipitate formed is collected, washed successively with hot water, methanol and diethyl ether, to yield the 4-methyl-2-phenylpyrazolo[4,3-c]quinolin-3(5H)-one, showing in the IR-spectrum peaks at 874, 867, 858, 850, 822, 780, 765, 756, 750, 740 and 722 cm-1. Analogously the 4-methyl-2-(p-chlorophenyl)-pyrazolo[4-3,-c]quinolin-3(5H)-one is prepared, melting at 349°-350°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04312870 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-7b46845f285841a28ed0369a24ca0a90 |
| Source note | uspto-grants-1982_01 |