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HRID 581093作成日:2026年10月25日

1,1'-Carbonyldiimidazole → 5-Chloro-3-(4-(2-methyl-4-thiazolyl)-2-thenoyl)-2-oxindole-1-carboxamide

https://huagongshe.com/reaction/581093

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物5-Chloro-2-oxo-2,3-dihydro-1H-indole-1-carboxamideHCID 9859159—
反応物4-(2-Methylthiazol-4-yl)-2-thiophenecarboxylic acidHCID 15007357—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物5-Chloro-3-(4-(2-methyl-4-thiazolyl)-2-thenoyl)-2-oxindole-1-carboxamideHCID 9823291—

反応手順

The title compound was prepared according to the procedure of Example 55. A 1.25 g (5.55 mmoles) sample of 4-(2-methyl-4-thiazolyl)-2-thiophenecarboxylic acid (prepared as described in Example 18) was converted to the acyl imidazole by reaction with 0.98 g (6.05 mmoles) of 1,1'-carbonyldiimidazole in 15 ml of N,N-dimethylformamide. After complete reaction this solution was transferred to an addition funnel and slowly added 1.06 g (5.04 mmoles) of 5-chloro-2-oxindole-1-carboxamide and 1.66 g (13.59 mmoles) of 4-(N,N-dimethylamino)pyridine in 50 ml of N,N-dimethyl-formamide. Acidic workup followed by filtration and trituration with 2-butanone gave 0.50 g (1.20 mmoles) of title compound as a yellow solid, m.p. 238-241° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05919809
出典データセットuspto-grants-1999_07
ORD IDord-f238a35d5b55441d94ad73a82029f2f6
出典メモuspto-grants-1999_07