HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → HCID 178485838, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 178507701 | HCID 178507701 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178485838 | HCID 178485838 | — |
Reaction Steps
The mixture of 0.7 g of 2-(p-aminophenyl)-pyrazolo[4,3-c]quinolin-3(5H)-one, 1.4 g of methylisocyanate and 25 ml of methanol is refluxed for 7 hours and allowed to stand at room temperature overnight. It is evaporated, the residue treated with diluted aqueous sodium hydroxide and diethyl ether, the aqueous solution separated, washed with diethyl ether and its pH adjusted to 8.5 with ammonium chloride. The precipitate formed is collected, washed with methanol, then with diethyl ether and dried, to yield the 2-(p-methylcarbamoylaminophenyl)-pyrazolo[4,3-c]quinolin3(5H)-one, showing IR-peaks of 895, 869, 850, 825, 816, 812, 785, 780, 767 and 738 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04312870 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-837ed730d07647fa94d18adc23ae732e |
| Source note | uspto-grants-1982_01 |