HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467279Generated: October 30, 2026
Hexahydro-1,4-diazepine → HCID 19813641, compound
https://huagongshe.com/reaction/467279
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | 7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 483169 | — |
| Product | HCID 19813641 | HCID 19813641 | 40.2% |
Reaction Steps
A mixture of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid [J. Med. Chem., 23, 1358 (1980)] (2.7 g, 10 mmol) and homopiperzine, (5.0 g, 50 mmol) was heated at 140° C. for 51/2 hours. The excess homopiperazine was removed by distillation at 85°-95° C./10 mm Hg. The residue was triturated with water and filtered. The solid collected was dissolved in glacial acetic acid (1.5 mL), water (10 mL) was added, and the pH was adjusted to 8.0 with solid sodium bicarbonate. The resulting precipitate was collected by filtration, washed with water (3×5 mL) and air dried to give the product as a white crystalline solid (1.34 g, 40% yield): mp 196°-198° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05159077 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-5412d66051e14b5c86a99301e6629ce7 |
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| Source note | uspto-grants-1992_10 |
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