HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369320Generated: October 31, 2026
(S)-(+)-1-Aminopropan-2-ol → HCID 54417395, compound
https://huagongshe.com/reaction/369320
Participants
| Role | Name | HCID | Charge |
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| Reactant | (S)-(+)-1-Aminopropan-2-ol | HCID 7311736 | — |
| Reactant | 1-(3-Amino-4,6-difluorophenyl)-8-chloro-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid | HCID 10861999 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 54417395 | HCID 54417395 | 85.8% |
Reaction Steps
1-(5-Amino-2,4-difluorophenyl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (150 mg) and (S)-1-amino-2-propanol (150 mg) were added to pyridine (450 mg), and the mixture was stirred at 55° C. for 2.5 hours. The reaction mixture was concentrated under reduced pressure. A process of adding ethanol (2 ml) to the residue and then concentrating the mixture under reduced pressure was conducted twice repeatedly. Concentrated hydrochloric acid (150 mg) was added to the resultant residue, and the mixture was concentrated under reduced pressure. Ethanol (1 ml) was added to the resultant residue, and deposits were collected by filtration and washed with ethanol and diisopropyl ether in that order to obtain the title compound (147 mg) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06136823 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-308ec778500747699172b2c36c5f8aa6 |
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| Source note | uspto-grants-2000_10 |
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