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HRID 542274Erstellt: 25. Oktober 2026

Furo[3,4-b]quinoline-1,3-dione → 2-[(1-Carbamoyl-1,2-dimethylpropyl)carbamoyl]-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/542274

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFuro[3,4-b]quinoline-1,3-dioneHCID 4325463—
Edukt2-Amino-2,3-dimethylbutanamideHCID 9793773—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-[(1-Carbamoyl-1,2-dimethylpropyl)carbamoyl]-3-quinolinecarboxylic acidHCID 13474736—

Reaktionsschritte

A solution of 2,3-quinolinedicarboxylic anhydride (0.037 mol) in tetrahydrofuran (THF, 250 mL) is stirred at 5° C. under a drying tube, and a solution of 2-amino-2,3-dimethylbutyramide (0.037 mol) in THF (50 mL) added thereto, in small increments, over a 15 minute period. The reaction mixture is allowed to warm slowly to room temperature for an extended period of time, i.e. about 17 hours. The solvent is evaporated in vacuo to afford a gummy residue, which is triturated with hot ethyl acetate (400 mL) and then filtered to afford the desired 2-[(1-carbamoyl-1,2-dimethylpropyl)-carbamoyl]-3-quinolinecarboxylic acid, mp 172.5°-173.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04656283
Quelldatensatzuspto-grants-1987_04
ORD IDord-64fe55d68e0c4ce7b0d679c2af879df9
Quellennotizuspto-grants-1987_04