HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 178510016, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-Chloroquinoline-3-carboxylate | HCID 268963 | — |
| Reactant | 4-Hydrazinobenzonitrile | HCID 583784 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178510016 | HCID 178510016 | — |
Reaction Steps
38.5 ml of a 0.17 M solution of ethyl 4-chloroquinoline-3-carboxylate in xylene, and 0.96 g of p-cyanophenylhydrazine in 30 ml of xylene are mixed and heated at 115° to 120° for 3 hours. The mixture is then cooled to room temperature, and stirred with 20 ml of 1 N aqueous sodium hydroxide and sufficient water to dissolve all solids. The aqueous layer is separated, washed twice with diethyl ether, then treated with an aqueous solution of 1.07 g ammonium chloride, and the resulting precipitate is collected, washed with water and dried to yield the 2-(p-cyanophenyl)-pyrazolo[4,3-c]quinolin-3(5H)-one, showing peaks in the IR-spectrum at 885, 830, 780, 755 and 730 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04312870 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-84c550626ae847d5b32d950015eebc2e |
| Source note | uspto-grants-1982_01 |