HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344907Generated: October 29, 2026
2-(4-Methoxyphenyl)piperazine → HCID 54470582, compound
https://huagongshe.com/reaction/344907
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(4-Methoxyphenyl)piperazine | HCID 2771753 | — |
| Reactant | 1-Cyclopropyl-3-ethoxycarbonyl-7,8-difluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine | HCID 14853340 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 54470582 | HCID 54470582 | 70% |
Reaction Steps
A suspension of 1-cyclopropyl-3-ethoxycarbonyl-7,8-difluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine (2 g) and (RS)-3-(4-methoxyphenyl)piperazine (2.3 g) in dimethyl sulphoxide (20 cc) is heated to a temperature in the region of 90° C. for 1 hour and a half. After cooling to approximately 20° C., the insoluble matter is drained, washed with water (3×15 cc) and recrystallized in a mixture of ethanol (100 cc) and dimethylformamide (25 cc). (RS)-1-Cyclopropyl-3-ethoxycarbonyl-7-fluoro-8-[3-(4-methoxyphenyl)-1-piperazinyl]-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine (2.1 g) is obtained in the form of a yellow solid, m.p. 199° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05053509 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-9d2d931f61ac40949b4da1b73f1557e4 |
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| Source note | uspto-grants-1991_10 |
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