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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165603Generated: November 3, 2026

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

https://huagongshe.com/reaction/1165603

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 numberUS04910327
Source datasetuspto-grants-1990_03
ORD IDord-f20a057acc4d40b1b5435b0a37f6b99a
Source noteuspto-grants-1990_03