Reaktion #1705789

ord-2721e0a3cf524cd6a44583e59c0a886d

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigePrepared

Vorschrift

Prepared according to procedure M using 6-bromo-2′,3′,5′,6′-tetrahydrospiro-[indoline-3,4′-pyran] (0.3 g, 1.12 mmol) and 4,6-dichloro-7-methoxy-2,3-dimethylquinoline (0.3152 g, 1.23 mmol) to give 6-bromo-1-(6-chloro-7-methoxy-2,3-dimethyl-4-quinolinyl)-1,2,2′,3′,5′,6′-hexahydrospiro[indole-3,4′-pyran] as a: 1H NMR (500 MHz, DMSO-d6) δ ppm 7.65 (1H, s), 7.58 (1H, s), 7.21 (1H, d, J=8.1 Hz), 6.82 (1H, dd, J=7.8, 1.7 Hz), 5.90 (1H, d, J=1.7 Hz), 3.96-4.05 (4H, m), 3.82-3.92 (3H, m), 3.41-3.53 (2H, m), 2.66 (3H, s), 2.17 (3H, s), 1.95-2.06 (2H, m), 1.85 (1H, dd, J=13.4, 1.7 Hz), 1.72 (1H, dd, J=13.3, 1.8 Hz); Mass Spectrum (ESI) m/e=487.0 [M+1 (79Br)] and 489.1 [M+1 (81Br)].

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08765940B2uspto-grants-2014_07