HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1742939Erstellt: 24. Oktober 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-Cyclopropyl-6-fluoro-7-(3-(1, 2, 3-triazol-1-yl) pyrrolidin-1-yl]-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid
https://huagongshe.com/de/reaction/1742939
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | 1-Cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid | HCID 5210422 | — |
| Edukt | 1-(pyrrolidin-3-yl)-1H-1,2,3-triazole hydrochloride | HCID 19005943 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 1-Cyclopropyl-6-fluoro-7-(3-(1, 2, 3-triazol-1-yl) pyrrolidin-1-yl]-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid | HCID 54338418 | — |
Reaktionsschritte
A mixture of 1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid (120 mg, 0.486 mmol), DBU (190 mg, 1.25 mmol), 3-(1,2,3-triazol-1-yl)pyrrolidine hydrochloride (216 mg, 1.25 mmol) in pyridine (8 ml) was heated at 80° C. for 18 h. The reaction mixture was concentrated and treated with water. The separated solid was collected by filtration, washed with water and acetonitrile to give light brown solid. Yield: 71 mg (38%), m.p. 284° C. (dec). 1H NMR (TFA) δ: 1.5 (m, 4H), 3.0 (m, 2H), 4.0 (m, 4H), 4.65 (bs, 1H), 5.9 (bs, 1H), 7.5 (d, 1H),8.20 (d, 1H), 8.6 (s, 1H), 8.7 (s, 1H), 9.2 (S, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05342846 |
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| Quelldatensatz | uspto-grants-1994_08 |
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| ORD ID | ord-68661dba03084cbb93a56396af9c98a9 |
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| Quellennotiz | uspto-grants-1994_08 |
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