Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106257Generated: October 31, 2026

Methyl Isocyanate → HCID 178485838, compound

https://huagongshe.com/reaction/1106257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl IsocyanateHCID 12228—
ReactantHCID 178507701HCID 178507701—
SolventMethanolHCID 887—
ProductHCID 178485838HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04312870
Source datasetuspto-grants-1982_01
ORD IDord-837ed730d07647fa94d18adc23ae732e
Source noteuspto-grants-1982_01