Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Aziridine | HCID 9033 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 3-Phenylindole | HCID 96502 | — |
| Edukt | 2-Trifluoromethyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridine | HCID 57474036 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 11504035 | HCID 11504035 | 72,3% |
Reaktionsschritte
To a solution of 48 mg (0.25 mmol) of 3-phenyl-1H-indole in 3 mL of DMF was added 28 mg (0.7 mmol) of 60% sodium hydride in mineral oil. The mixture stirred until hydrogen evolution ceased and then 73 mg (0.25 mmol) of 2-trifluoromethyl-1-(2,4,6-trimethylbenzenesulfonyl)aziridine was added. The reaction was monitored by TLC (20% EtOAc-hexanes and 50% hexanes-CH2Cl2) indicating starting aziridine was consumed. After 30 minutes, the mixture was quenched with 7 mL of saturated aqueous ammonium chloride solution and extracted with three 7 mL portions of ethyl acetate. The combined organic layers were washed with three 7 mL portions of saturated aqueous ammonium chloride solution and three 7 mL portions of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was triturated with ether to afford 88 mg (72%) of the title compound. MS: m/z 487.59 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07635711B2 |
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| Quelldatensatz | uspto-grants-2009_12 |
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| ORD ID | ord-aa2b08c421de4568a875b676811756a6 |
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| Quellennotiz | uspto-grants-2009_12 |
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