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HRID 62648作成日:2026年10月26日

Dimethylformamide → ethyl 4,6-dicyano-1H-indole-2-carboxylate

https://huagongshe.com/reaction/62648

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物ethyl 4,6-dichloro-1H-indole-2-carboxylateHCID 2736407—
反応物2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
反応物HCID 178514179HCID 178514179—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒AmmoniaHCID 222—
溶媒WaterHCID 962—
生成物ethyl 4,6-dicyano-1H-indole-2-carboxylateHCID 8999532132%

反応条件

温度160 °C

反応手順

To an argon purged solution of ethyl 4,6-dichloro-1H-indole-2-carboxylate (I-1c: 1 g, 3.89 mmol) in DMF (8 mL) were added dicyanozinc (1.37 g, 11.67 mmol), Pd2(dba)3 (356 mg, 0.389 mmol) followed by Xphos (166 mg. 0.389 mmol), the mixture was then stirred in microwave at 160° C. for 14 h. The resultant reaction mixture was allowed to cool to room temperature, diluted with water (10 mL) and ammonia solution (2 mL; Specific Gravity 0.91). The aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic layer was washed with water, brine, dried over anhydrous Na2SO4 solution and concentrated. The crude compound was purified by column chromatography over silica gel (100-200 mesh) using a solvent gradient of 6% ethyl acetate in chloroform as eluent to afford 300 mg (32%) of ethyl 4,6-dicyano-1H-indole-2-carboxylate (I-2a) as a brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447039B2
出典データセットuspto-grants-2016_09
ORD IDord-41af761c9581408a806f6f2bca9ca8bd
出典メモuspto-grants-2016_09