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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 981188Erstellt: 26. Oktober 2026

Hydrazinecarboxaldehyde, 1-methyl- → 8-chloro-3-ethoxycarbonyl-7-fluoro-1-(N-formyl-N-methylamino)-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine

https://huagongshe.com/reaction/981188

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrazinecarboxaldehyde, 1-methyl-HCID 12962—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktEthyl 2-(2,7-dichloro-6-fluoroquinoline-3-carbonyl)-3-dimethylaminoacrylateHCID 54015905—
LösungsmittelEthanolHCID 702—
Produkt8-chloro-3-ethoxycarbonyl-7-fluoro-1-(N-formyl-N-methylamino)-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridineHCID 1470055186,9%

Reaktionsschritte

The 8-chloro-3-ethoxycarbonyl-7-fluoro-1-(N-formyl-N-methylamino)-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine is prepared under the conditions of Example 1 but starting from 19.25 g of ethyl 2-(2,7-dichloro-6-fluoroquinoline-3-carbonyl)-3-dimethylaminoacrylate, 4.05 g of N-formyl-N-methylhydrazine and 1.6 g of DBU in 200 cm3 of ethanol. 16.4 g of 8-chloro-3-ethoxycarbonyl-7-fluoro-1-(N-formyl-N-methylamino)-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine are obtained in the form of a colourless solid melting at 296°-298° C., which can be used for the subsequent steps without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04990515
Quelldatensatzuspto-grants-1991_02
ORD IDord-e48276b1b22d4636b859dcecbde9183f
Quellennotizuspto-grants-1991_02