HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494741Generated: October 30, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 14795764, compound
https://huagongshe.com/reaction/1494741
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 1-Cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid | HCID 5210422 | — |
| Reactant | 5-Chloroisoindoline | HCID 14795866 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14795764 | HCID 14795764 | 62.6% |
Reaction Steps
A mixture of 136 mg of 1-cyclopropyl-6,7-difluoro-1,4- dihydro-4-oxoquinoline-3-carboxylic acid, 123 mg of 5-chloroisoindoline, 122 mg of DBU, and 1.5 ml of anhydrous DMF was heated at 110° C. for 1.5 hours while stirring. The resulting reaction mixture was evaporated under reduced pressure to dryness. 20 ml of chloroform and 10 ml of 5% acetic acid were added to the residue thus obtained, and the mixture was stirred. The deposited crystals were collected by filtration and washed with water and then ethanol. The chloroform layer was separated, and washed with water, dried over anhydrous sodium sulfate, and condensed. The residue was crystallized by the addition of hot ethanol. After cooling the mixture, the crystals were collected by filtration. These crystals, combined with the crystals obtained above, were recrystallized from a mixed solvent of chloroform, methanol, and ethanol to obtain 128 mg of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05026856 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-fe2eabe3763c438ba8b5169e87813ac7 |
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| Source note | uspto-grants-1991_06 |
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