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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650113Generated: October 28, 2026

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

https://huagongshe.com/reaction/1650113

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 (0.037 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923504
Source datasetuspto-grants-1990_05
ORD IDord-ce49a03c36fe4c31b7307cd911b3fe2d
Source noteuspto-grants-1990_05