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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084401Generated: October 30, 2026

1-Methylpiperazine → HCID 14853346, compound

https://huagongshe.com/reaction/1084401

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant1-Cyclopropyl-3-ethoxycarbonyl-7,8-difluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridineHCID 14853340—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDiisopropyl EtherHCID 7914—
ProductHCID 14853346HCID 1485334674.4%

Reaction Steps

A suspension of 1.2 g of 1-cyclopropyl-3-ethoxycarbonyl-7,8-difluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine in 1.4 g of 1-methylpiperazine and 20 cm3 of dimethyl sulphoxide is heated at a temperature close to 95° C. for 45 minutes. After cooling to a temperature close to 20° C., the reaction mixture is diluted with 100 cm3 of water and extracted with 3 times 30 cm3 of trichloromethane. The combined organic extracts are washed with 3 times 30 cm3 of water, dried over magnesium sulphate, filtered and concentrated under reduced pressure (20 kPa) at a temperature close to 50° C. The solid obtained is taken up in 20 cm3 of diisopropyl ether, drained, washed with 10 cm3 of the same solvent and recrystallized from 150 cm3 of ethyl acetate. 1.1 g of 1-cyclopropyl-3-ethoxycarbonyl-7-fluoro-8-(4-methyl-1-piperazinyl)-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine are obtained in the form of a yellow solid melting at 223° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004745
Source datasetuspto-grants-1991_04
ORD IDord-f11c3e731cb24239a96cb802b9fbc254
Source noteuspto-grants-1991_04