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HRID 542274作成日:2026年10月26日

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

https://huagongshe.com/reaction/542274

反応式

関与物質

役割名称HCID仕込み量
反応物Furo[3,4-b]quinoline-1,3-dioneHCID 4325463—
反応物2-Amino-2,3-dimethylbutanamideHCID 9793773—
溶媒TetrahydrofuranHCID 8028—
生成物2-[(1-Carbamoyl-1,2-dimethylpropyl)carbamoyl]-3-quinolinecarboxylic acidHCID 13474736—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04656283
出典データセットuspto-grants-1987_04
ORD IDord-64fe55d68e0c4ce7b0d679c2af879df9
出典メモuspto-grants-1987_04