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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980556Generated: 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/980556

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 numberUS04638068
Source datasetuspto-grants-1987_01
ORD IDord-74aba897be064ddd950d3bd9e9e8af94
Source noteuspto-grants-1987_01