HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084401Generated: October 30, 2026
1-Methylpiperazine → HCID 14853346, compound
https://huagongshe.com/reaction/1084401
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 1-Cyclopropyl-3-ethoxycarbonyl-7,8-difluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine | HCID 14853340 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 14853346 | HCID 14853346 | 74.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05004745 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-f11c3e731cb24239a96cb802b9fbc254 |
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| Source note | uspto-grants-1991_04 |
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