Reaktion #8412

Reaktionsgleichung

N-tert-butyldimethylsilyl -4-chloroindole

KH2PO4

2-(dicyclohexylphosphino)-biphenyl

tert-BuONa

tert-butyl 1-piperazinecarboxylate

→

N-tert-Butyldimethylsilyl-4-(4-Boc-piperazinyl)-indole

Lösungsmittel

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe compound was prepared
2. 2
   Extraktionfollowed by extraction with toluene (2×100 mL)
3. 3
   Trocknendried (MgSO4)
4. 4
   Sonstigeevaporated
5. 5
   SonstigeThe residue was crystallized from heptane
6. 6
   Sonstigeto yield 124.4 g (79.6%)

Vorschrift

The compound was prepared according to Method 2 from N-tert-butyldimethylsilyl -4-chloroindole (100 g, 376 mmol, 1 equiv.), tert-butyl 1-piperazinecarboxylate (84 g, 451 mmol), Palladium(II) acetate (1.26 g., 5.62 mmol, 2%), 2-(dicyclohexylphosphino)-biphenyl (3.95 g., 11.28 mmol, 4 mol %), tert-BuONa (50 g, 520 mmol, 1.4 equiv.) in toluene. The solution was cooled to room temperature and KH2PO4 (150 mL, 13% aqueous solution) was added and pH was adjusted (pH=8–9) followed by extraction with toluene (2×100 mL), dried (MgSO4) and evaporated. The residue was crystallized from heptane to yield 124.4 g (79.6%). 1H NMR (CDCl3) δ 7.20 (d, J=8.4 Hz, 1 H), 7.13 (d, J=3.2 Hz, 1 H), 7.06 (t, 1 H), 6.60–6.57 (m, 2 H), 3.65 (t, 4 H), 3.16 (t, 4 H), 1.48 (s, 9 H), 0.91 (s, 9 H), 0.58 (s, 6 H); 13C NMR (CDCl3) δ 155.0; 145.5; 142.2; 129.9; 124.9; 122.0; 109.3; 107.2; 102.9; 79.8; 77.3; 51.5; 28.5; 26.4; 19.5; −3.8; MS (ESI) 416.4 (M+H).

Quelle