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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62648Generated: October 26, 2026

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

https://huagongshe.com/reaction/62648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactantethyl 4,6-dichloro-1H-indole-2-carboxylateHCID 2736407—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantHCID 178514179HCID 178514179—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventAmmoniaHCID 222—
SolventWaterHCID 962—
Productethyl 4,6-dicyano-1H-indole-2-carboxylateHCID 8999532132%

Reaction Conditions

Temperature160 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447039B2
Source datasetuspto-grants-2016_09
ORD IDord-41af761c9581408a806f6f2bca9ca8bd
Source noteuspto-grants-2016_09