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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613473Generated: October 29, 2026

Water → 2-tert-butoxycarbonyl-2,3-dihydro-1-methyl-6-nitro-1H-pyrazolo[4,3-c]quinolin-3-one

https://huagongshe.com/reaction/613473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-tert-butoxycarbonyl-2,3-dihydro-6-nitro-1H-pyrazolo[4,3-c]quinolin-3-oneHCID 19593009—
SolventDimethylformamideHCID 6228—
Product2-tert-butoxycarbonyl-2,3-dihydro-1-methyl-6-nitro-1H-pyrazolo[4,3-c]quinolin-3-oneHCID 1959250424.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of 2-tert-butoxycarbonyl-2,3-dihydro-6-nitro-1H-pyrazolo[4,3-c]quinolin-3-one (450 mg) and potassium carbonate (565 mg) in dimethylformamide was added methyl iodide (580 mg), and the mixture was stirred for 2 hours at 60° C. The mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (dichloromethane-ethyl acetate) to give 2-tert-butoxycarbonyl-2,3-dihydro-1-methyl-6-nitro-1H-pyrazolo[4,3-c]quinolin-3-one (114 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008230
Source datasetuspto-grants-1999_12
ORD IDord-20d13cec7a35481b8031dfa1ae4a7a69
Source noteuspto-grants-1999_12