HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289899Generated: October 31, 2026
Hydrochloric Acid → HCID 178522885, compound
https://huagongshe.com/reaction/2289899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | Ethyl 7-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 178469609 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178522885 | HCID 178522885 | — |
Reaction Steps
To a 0° C. solution of 4-chlorobenzylamine (0.52 mL) in 5 mL of toluene is added 2.13 mL of a 2.0 M solution of trimethylaluminum in toluene. The solution is stirred for 5 min at 0° C. and then a suspension of 0.50 g of ethyl 7-fluoro-4-hydroxy-3-quinolinecarboxylate (J. Med. Chem., 20, 1001 (1977)) in 5 mL of toluene is added. The solution is stirred at 0° C. for an additional 10 min and then it is stirred 18 h at 90° C. The mixture is cooled to 25° C. and it is poured onto a mixture of a large excess of 3 M hydrochloric acid and ice. After stirring the mixture vigorously for 30 min it is filtered. The solid is dissolved in 50 mL of warm glacial acetic acid and distilled water is added to the resulting solution until it is cloudy. The mixture is then allowed to stand for several hours at 5° C. Filtration of this mixture gives the desired amide as 150 mg of a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06093732 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-ab7f71f4bd584214b06ab8ee7c62385e |
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| Source note | uspto-grants-2000_07 |
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