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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 851007Erstellt: 24. Oktober 2026

Dimethylformamide → 1,4-Dihydro-4-oxo-8-[[(5-oxo-2-pyrrolidinyl)carbonyl]amino]-3-quinolinecarboxylic acid

https://huagongshe.com/de/reaction/851007

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktChlorotrimethylsilaneHCID 6397—
EduktL-Pyroglutamic AcidHCID 7405—
EduktTriethylamineHCID 8471—
EduktThionyl ChlorideHCID 24386—
Edukt8-Amino-4-hydroxyquinoline-3-carboxylic acidHCID 12866349—
LösungsmittelDichloromethaneHCID 6344—
Produkt1,4-Dihydro-4-oxo-8-[[(5-oxo-2-pyrrolidinyl)carbonyl]amino]-3-quinolinecarboxylic acidHCID 1313687253,9%

Reaktionsschritte

A mixture of 3.87 g (30 mmol) of 5-oxo-L-proline, 2.19 ml (30 mmol) of thionyl chloride, 2.32 ml (30 mmol) of dimethylformamide, and 75 ml of dichloromethane is stirred with cooling for 1 hour. A mixture of 4.08 g (20 mmol) 8-amino-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 8.4 ml (60 mmol) of triethylamine, 7.6 ml (60 mmol) of chlorotrimethylsilane, and 100 ml of dichloromethane is stirred at room temperature for 40 minutes and then is cooled to 0°. The cold acid chloride solution is added to the cold silylated quinoline and the mixture is stirred with cooling for 4 hours and at room temperature overnight. The reaction mixture is evaporated to dryness and the residue is treated with ethanol to give 3.40 g of 1,4-dihydro-4-oxo-8-[[(5-oxo-2-pyrrolidinyl)carbonyl]amino]-3-quinolinecarboxylic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04382089
Quelldatensatzuspto-grants-1983_05
ORD IDord-bbb0dffa458949ceaefef443213fc58e
Quellennotizuspto-grants-1983_05