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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622166Generated: October 27, 2026

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

https://huagongshe.com/reaction/622166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuro[3,4-b]quinoline-1,3-dioneHCID 4325463—
Reactant2-Amino-2,3-dimethylbutanamideHCID 9793773—
SolventTetrahydrofuranHCID 8028—
Product2-[(1-Carbamoyl-1,2-dimethylpropyl)carbamoyl]-3-quinolinecarboxylic acidHCID 13474736—

Reaction Steps

A solution of 2,3-quinolinedicarboxylic anhydride (0.37 mol) in tetrahydrofuran (THF, 250 mL) is stirred at 5° C. under a drying tube, and a solution of 2-amino-2,3-dimethylbutyramide (0.37 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04769462
Source datasetuspto-grants-1988_09
ORD IDord-20bc0f060c4749d48b1c0877fc3ce242
Source noteuspto-grants-1988_09