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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106256Generated: October 31, 2026

Formaldehyde → HCID 178482194, compound

https://huagongshe.com/reaction/1106256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantAcetonitrileHCID 6342—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178507701HCID 178507701—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 178482194HCID 178482194—

Reaction Steps

To the mixture of 1.4 g of 2-(p-aminophenyl)-pyrazolo-[4,3-c]quinolin-3(5H)-one, 4.1 ml of 37% aqueous formaldehyde, 1.0 g of sodium cyanoborohydride and 20 ml of acetonitrile, 0.6 g of glacial acetic acid are added while stirring. Stirring is continued overnight at room temperature and the mixture diluted with water. The precipitate formed is dissolved in diluted sodium hydroxide, the aqueous solution washed with diethyl ether and its pH adjusted to 8.5 by addition of aqueous ammonium chloride. The precipitate formed is collected, washed with methanol, then with diethyl ether and dried to yield the 2-(p-methylaminophenyl)-pyrazolo[4,3-c]quinolin-3(5H)-one melting at 302°-304°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04312870
Source datasetuspto-grants-1982_01
ORD IDord-0a35d5268397474486f4526317186729
Source noteuspto-grants-1982_01