HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907195Generated: October 26, 2026
Ethyl Acetate → diethyl [4-(3-cyano-6-ethoxy-1-ethyl-1H-indol-2-yl)-phenyl]-phosphoramidate
https://huagongshe.com/reaction/907195
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(4-aminophenyl)-6-ethoxy-1-ethyl-1H-indole-3-carbonitrile | HCID 59425274 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | diethyl [4-(3-cyano-6-ethoxy-1-ethyl-1H-indol-2-yl)-phenyl]-phosphoramidate | HCID 59425449 | 51% |
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) was stirred at ambient temperature for 12 hours, then heated to 80° C. for an additional 24 hours. The solution was cooled and poured into 50 mL of ethyl acetate. This was washed with water and saturated brine (50 mL each), then dried over anhydrous magnesium sulfate, filtered and evaporated. The residual material was 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08013006B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-e1d8cc8c1bd64062b18274c1ea2a0cbe |
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| Source note | uspto-grants-2011_09 |
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