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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62661Generated: October 30, 2026

Aniline → 4-methyl-N-((1R,2S)-2-methylcyclohexyl)-6-(phenylamino)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/62661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Reactant6-bromo-4-methyl-N-((1R,2S)-2-methylcyclohexyl)-1H-indole-2-carboxamideHCID 73291801—
ReactantHCID 178418922HCID 178418922—
Catalystpalladium(II) acetateHCID 167845—
SolventO-XyleneHCID 7237—
Product4-methyl-N-((1R,2S)-2-methylcyclohexyl)-6-(phenylamino)-1H-indole-2-carboxamideHCID 7350795331%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 6-bromo-4-methyl-N-((1R,2S)-2-methylcyclohexyl)-1H-indole-2-carboxamide (4AH: 500 mg, 1.43 mmol) in xylene (7.5 mL) were added Pd(OAc)2 (58 mg, 0.26 mmol), JohnPhos (51 mg, 0.17 mmol), tBuOK (644 mg, 5.74 mmol) and aniline (802 mg, 8.62 mmol). The resulting mixture was purged with argon for 10 minutes and then heated at 100° C. for 3 h in sealed tube. The reaction mixture was partitioned between ethyl acetate and water. The organic layer separated and washed with brine and dried over Na2SO4, concentrated. The crude product was purified by column chromatography followed by preparative HPLC to obtain 160 mg of 4-methyl-N-((1R,2S)-2-methylcyclohexyl)-6-(phenylamino)-1H-indole-2-carboxamide (6A: 30%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447039B2
Source datasetuspto-grants-2016_09
ORD IDord-f5d8ae6b18cc4fb39193805344825bf0
Source noteuspto-grants-2016_09