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HRID 1259845作成日:2026年10月27日

Pyridine → Quinoline carboxamide derivative 1

https://huagongshe.com/reaction/1259845

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物5-(Furan-2-yl)-1,3,4-oxadiazol-2-amineHCID 202185—
反応物2-Phenylquinoline-4-carbonyl chlorideHCID 2760409—
溶媒MethanolHCID 887—
生成物Quinoline carboxamide derivative 1HCID 425323643.1%

反応条件

温度60 °C

反応手順

2-phenyl-4-quinolinecarbonyl chloride (2.00 g, 7.47 mmol) was added in small portions to a pyridine (40 mL) solution of commercially available 2-amino-5-(2-furyl)-1,3,4-oxadiazole (1.69 g, 11.2 mmol), and the mixture was heated with stirring at 60° C. for 6 hours. To the reaction solution, methanol was added, and the solvent was distilled off. The obtained residue was triturated by the addition of water. The deposited crystal was collected by filtration, washed with methanol and then with ethyl acetate, and then recrystallized from DMF-methanol to obtain the title compound (1.23 g, 3.22 mmol) as a light brown powder (yield: 43%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08466290B2
出典データセットuspto-grants-2013_06
ORD IDord-ee5b437691344d60bdb8eed564e0619d
出典メモuspto-grants-2013_06