Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | m-Nitroacetophenone | HCID 8494 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | n-Cyclohexylpiperidine-4-carboxamide | HCID 12410238 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | HCID 131736797 | HCID 131736797 | 15% |
Reaktionsschritte
Piperidine-4-carboxylic acid cyclohexylamide (1.5 g 7.132 mmol) and 3-nitroacetophenone (1.77 g, 10.7 mmol) are dissolved in MeOH (40 mL). Tetraisopropyl-orthotitanate (3.167 mL, 10.7 mmol) is added and the mixture is stirred at RT for 18 h. NaBH4 (539.6 mg, 14.3 mmol) is added carefully. The mixture is evaporated under reduced pressure. DCM (25 mL) and water (25 mL) are added, following by 1 M NaOH solution (50 mL). The organic phase is separated and the aqueous phase is extracted with DCM (25 mL). The combined organic phases are dried over MgSO4, filtered and concentrated. The crude residue is purified by flash chromatography on silica gel using a gradient of heptane/EtOAc 4:1 to EtOAc 100%. After concentration of the product-containing fractions, the title compound (0.375 g, 15%) is obtained as a colorless solid LC-MS A: tR=0.64 min; [M+H]+=360.26.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09428456B2 |
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| Quelldatensatz | uspto-grants-2016_08 |
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| ORD ID | ord-40ff7817415c40428cd748c90186e540 |
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| Quellennotiz | uspto-grants-2016_08 |
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