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HRID 1699955作成日:2026年10月25日

1-Butanesulfonamide → 6-(1-n-Butanesulfonylcarbamoyl)-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazolone

https://huagongshe.com/reaction/1699955

反応式

関与物質

役割名称HCID仕込み量
反応物1-ButanesulfonamideHCID 18460—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物6-Carboxy-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazoloneHCID 22387851—
溶媒DimethylformamideHCID 6228—
生成物6-(1-n-Butanesulfonylcarbamoyl)-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazoloneHCID 2238775729.2%

反応手順

In the same manner as in Example 1, N,N′-carbonyldiimidazole (0.290 g) was added to a mixture of 6-carboxy-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazolone (0.314 g) and N,N-dimethylformamide (9 ml), and the mixture was stirred at room temperature for 1 hr. 1-n-Butanesulfonamide (0.246 g) and DBU (0.273 g) were added and the mixture was stirred at 100° C. for 16 hr. The solvent was evaporated and the resulting mixture was extracted with chloroform and water. The organic layer was concentrated and the residue was purified by preparative thin layer chromatography to give 6-(1-n-butanesulfonylcarbamoyl)-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazolone (0.123 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06348474B1
出典データセットuspto-grants-2002_02
ORD IDord-d23aa593f1a24b49a951c0428c7c0baa
出典メモuspto-grants-2002_02