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HRID 1514911作成日:2026年10月25日

2-Aminoquinoline → 2-(2,6-dichlorophenyl)-6,7-difluoro-3H-benzoimidazole-5-carboxylic acid quinolin-2-ylamide

https://huagongshe.com/reaction/1514911

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminoquinolineHCID 11379—
反応物DiisopropylethylamineHCID 81531—
反応物2-(2,6-dichlorophenyl)-6,7-difluoro-3H-benzoimidazole-5-carbonyl chlorideHCID 86651264—
溶媒TetrahydrofuranHCID 8028—
生成物2-(2,6-dichlorophenyl)-6,7-difluoro-3H-benzoimidazole-5-carboxylic acid quinolin-2-ylamideHCID 66965220—

反応条件

温度60 °C

反応手順

To a stirred suspension of 2-(2,6-dichlorophenyl)-6,7-difluoro-3H-benzoimidazole-5-carbonyl chloride (150 mg, 0.38 mmol) and quinolin-2-ylamine (55 mg, 0.38 mmol) in THF (10 mL) was added DIPEA (0.2 ml, 1.14 mmol) and the solution was heated at 60° C. for 4 days. The reaction was quenched with water and aqueous layer was extracted with EtOAc. The organic layer was washed with water, brine, dried with MgSO4, and filtered. The solvent was removed under reduced pressure and the residue was purified by flash chromatography using a gradient of heptane/EtOAc (4:1 to 100% EtOAc) to give 2-(2,6-dichlorophenyl)-6,7-difluoro-3H-benzoimidazole-5-carboxylic acid quinolin-2-ylamide as a white solid. 1H NMR (DMSO-d6, 400 MHz): δ 13.67 (s, 1H), 11.26 (s, 1H), 8.47 (d, 1H), 8.41 (d, 1H), 7.98 (d, 1H), 7.87 (d, 1H), 7.81 (d, 1H), 7.77 (m, 4H), 7.56 (m, 1H). MS (m/z) 469.1 (M+1); Retention time: 1.51 min (Method 10).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08222248B2
出典データセットuspto-grants-2012_07
ORD IDord-513d97a00f5c474da0ed683d757e2c3e
出典メモuspto-grants-2012_07