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HRID 640977作成日:2026年10月25日

Thionyl Chloride → 5-Chloro-1,3-dimethyl-1H-pyrazole-4-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide

https://huagongshe.com/reaction/640977

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物5-chloro-1,3-dimethyl-1H-pyrazole-4-carboxylic acidHCID 2779652—
反応物6-(3-Amino-benzoyl)-1,3-dihydro-indol-2-oneHCID 59256478—
溶媒TetrahydrofuranHCID 8028—
生成物5-Chloro-1,3-dimethyl-1H-pyrazole-4-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amideHCID 8661041872%

反応条件

温度79 °C

反応手順

A dry 25 mL flask was charged with 5-Chloro-1,3-dimethyl-1H-pyrazole-4-carboxylic acid (0.180 g, 0.873 mmol) and thionyl chloride (10 mL) and allowed to stir at 79° C. for 2 h. The thionyl chloride was then removed by rotary evaporation. The crude acid chloride dissolved in THF (5 mL). 6-(3-Amino-benzoyl)-1,3-dihydro-indol-2-one (as prepared in Example 40, 0.200 g, 0.794 mmol) was added to the THF solution of the acid chloride, and the mixture was allowed to reflux for 2 h. The reaction mixture was then allowed to cool to room temperature and the precipitate was filtered and washed with THF (˜5 mL) affording pure 5-Chloro-1,3-dimethyl-1H-pyrazole-4-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (0.233 g, 0.571 mmol, 72%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07692005B2
出典データセットuspto-grants-2010_04
ORD IDord-6e4c16b4654b47e2afb3c8da21984ad9
出典メモuspto-grants-2010_04