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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981910Generated: October 31, 2026

Methylamine → 2(1H)-Quinolinone, 1-butyl-4-(methylamino)-3-nitro-

https://huagongshe.com/reaction/981910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant2(1H)-Quinolinone, 1-butyl-4-chloro-3-nitro-HCID 9970925—
SolventTetrahydrofuranHCID 8028—
Product2(1H)-Quinolinone, 1-butyl-4-(methylamino)-3-nitro-HCID 1008478087%

Reaction Steps

11 g (0.039 mole) of Compound d obtained in Reference Example 4 was dissolved in 100 ml of tetrahydrofuran, and 30 ml (0.39 mole) of 40% methylamine was added with ice cooling, followed by stirring at room temperature for one hour. Then, the solvent was evaporated under reduced pressure, and water was added to the residues. The precipitate was collected by filtration and dried, to afford 9.2 g of Compound w (yield: 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994468
Source datasetuspto-grants-1991_02
ORD IDord-f3f84304477a4b1daecbafdedaab4c43
Source noteuspto-grants-1991_02