Reaktion #61585

ord-4df14f6fbcf44638a3c78e6c4345b0f8

Reaktionsgleichung

O=C1NCCc2c(-c3ccccc3)[nH]c3cccc1c23
Compound 12
O=C1NCCc2c(-c3ccccc3)[nH]c3cccc1c23
2-Phenyl-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol-6-one
OB(O)c1cccc(Cl)c1
3-chlorophenylboronic acid
O=C1NCCc2c(-c3cccc(Cl)c3)[nH]c3cccc1c23
2-(3-chlorophenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

In a manner similar to that described for Compound 12, the tricyclic bromide (200 mg, 0.75 mmol) and 3-chlorophenylboronic acid (130 mg, 0.83 mmol) were coupled to yield 2-(3-chlorophenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one, 151 mg (67%), as a shiny pale-yellow solid. mp 147-149° C.; 1H NMR (300 MHz, d6-DMSO) δ 3.06 (m, 2H), 3.39 (m, 2H), 7.24 (app t, 1H, J=7.8 Hz), 7.46 (m, 1H), 7.58 (m, 4H), 7.70 (m, 2H), 7.64 (m, 1H), 8.11 (br t, 1H), 11.68 (br s, 1H); MS (FAB, MH+) 297; Anal. (C17H13N2OCl.0.9 H2O) C, H, N.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07429578B2uspto-grants-2008_09