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HRID 62648생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/62648

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물ethyl 4,6-dichloro-1H-indole-2-carboxylateHCID 2736407—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물HCID 178514179HCID 178514179—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매AmmoniaHCID 222—
용매WaterHCID 962—
생성물ethyl 4,6-dicyano-1H-indole-2-carboxylateHCID 8999532132%

반응 조건

온도160 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447039B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-41af761c9581408a806f6f2bca9ca8bd
출처 메모uspto-grants-2016_09