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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009628Generated: October 26, 2026

Ethyl Acetate → diethyl [4-(3-cyano-6-ethoxy-1-ethyl-1H-indol-2-yl)-phenyl]-phosphoramidate

https://huagongshe.com/reaction/1009628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiethyl chlorophosphateHCID 13139—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(4-aminophenyl)-6-ethoxy-1-ethyl-1H-indole-3-carbonitrileHCID 59425274—
Solvent1,4-DioxaneHCID 31275—
Productdiethyl [4-(3-cyano-6-ethoxy-1-ethyl-1H-indol-2-yl)-phenyl]-phosphoramidateHCID 5942544951%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 2-(4-aminophenyl)-6-ethoxy-1-ethyl-1H-indole-3-carbonitrile (148 mg, 0.484 mmol), diethyl chlorophosphate (0.086 mL, 0.58 mmol) and diisopropylethylamine (0.10 mL, 0.57 mmol) in 1,4-dioxane (5 mL) is stirred at ambient temperature for 12 hours, then heated to 80° C. for an additional 24 hours. The solution is cooled and poured into 50 mL of ethyl acetate. This is washed with water and saturated brine (50 mL each), then dried over anhydrous magnesium sulfate, filtered and evaporated. The residual material is separated by flash chromatography (eluting 2/1 ethyl acetate/hexane on silica gel 60) to afford diethyl [4-(3-cyano-6-ethoxy-1-ethyl-1H-indol-2-yl)-phenyl]-phosphoramidate (108 mg, 0.245 mmol, 51%) as a white powder after evaporation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973069B2
Source datasetuspto-grants-2011_07
ORD IDord-2df52b5814d24e8c8a7e99ee72981998
Source noteuspto-grants-2011_07