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HRID 1067989作成日:2026年10月26日

Dimethylformamide → N-[(4-chlorophenyl)methyl]-1-methyl-6-(1,4-oxazepan-4-ylmethyl)-4-oxo-quinoline-3-carboxamide

https://huagongshe.com/reaction/1067989

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物2,4,6-TrimethylpyridineHCID 7953—
反応物Methanesulfonyl chlorideHCID 31297—
反応物N-(4-Chlorobenzyl)-6-(hydroxymethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamideHCID 15516933—
触媒4-(Dimethylamino)pyridineHCID 14284—
生成物N-[(4-chlorophenyl)methyl]-1-methyl-6-(1,4-oxazepan-4-ylmethyl)-4-oxo-quinoline-3-carboxamideHCID 1607386231%

反応手順

Methanesulfonyl chloride (0.080 mL) is added to a cold (0° C.) solution of N-(4-chlorobenzyl)-6-(hydroxymethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamide (330 mg) from Preparation No. 10, DMAP (19.1 mg), and 2,4,6-collidine (0.14 mL) in anhydrous DMF (15.7 mL). The mixture is stirred at room temperature until the starting material is consumed and a solution of 1,4-oxepane (0.963 g) from Preparation No. 33 in anhydrous DMF (3 mL) is added. The reaction mixture is heated to 56° C. for 1.5 h. The mixture is cooled to room temperature and the product is precipitated by addition of water (125 mL). The solid was adsorbed onto silica and purified by column chromatography (eluent 100% CH2Cl2 (1 L), 1% MeOH in CH2Cl2 (2 L), 1.5% MeOH in CH2Cl2 (1 L), 2% MeOH in CH2Cl2 (3 L)). Fractions homogenous by TLC are combined and concentrated to afford 124.5 mg (31%) of the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06248739B1
出典データセットuspto-grants-2001_06
ORD IDord-27c11d60dbcb4226807ccb1a0fc16785
出典メモuspto-grants-2001_06