Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-tert-Butylbenzoyl chloride | HCID 74372 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | (S)-methyl 2-amino-3-(4-cyanophenyl)propanoate | HCID 54521608 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 73939388 | HCID 73939388 | 88% |
Reaktionsschritte
Prepared using General Procedure 3: To the solution of (S)-methyl 2-amino-3-(4-cyanophenyl)propanoate (789.2 mg, 3.32 mmol) in DCM (15 mL) and DIEA (1.29 g, 9.96 mmol) was added 4-(tert-butyl)benzoyl chloride (981.3 mg, 4.99 mmol) at RT. The reaction was stirred for 2 h and the reaction was partitioned between DCM and saturated aqueous NaHCO3. The organic layer was dried over MgSO4 and concentrated. The crude product was purified by chromatography (EA/hexanes) to afford 1.06 g (88%) of (S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-cyanophenyl)propanoate. LCMS-ESI (m/z) calculated for C22H24N2O3: 364.2; found 365.3 [M+H]+, tR=3.55 min (Method 1). 1H NMR (400 MHz, CDCl3) δ 8.81 (d, J=8.0 Hz, 1H), 7.85-7.60 (m, 4H), 7.49 (dd, J=15.1, 8.4 Hz, 4H), 4.85-4.60 (m, 1H), 3.65 (s, 3H), 3.30-3.23 (m, 1H), 3.18 (dd, J=13.7, 10.6 Hz, 1H), 1.29 (s, 9H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08778923B2 |
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| Quelldatensatz | uspto-grants-2014_07 |
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| ORD ID | ord-81aabca718ec42d889984d77301fbf24 |
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| Quellennotiz | uspto-grants-2014_07 |
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