Reaktion #61595

ord-01063a03f97e4da8869143999e1966c7

Reaktionsgleichung

O=C1NCCc2c(Br)[nH]c3cccc1c23
2-bromo-3,4,5,6-tetrahydro-azepino[5,4,3-cd]indol-6-one
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Oc1ccc(I)cc1
4-iodophenol
CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C
diboron pinacol ester
CC(=O)[O-].[K+]
potassium acetate
O=C1NCCc2c(-c3ccc(O)cc3)[nH]c3cccc1c23
2-(4-hydroxy-phenyl)-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 YY, 4-iodophenol (220 mg, 1.00 mmol), diboron pinacol ester (279 mg, 1.10 mmol), 1,1′-bis(diphenyl phosphino)ferrocenedichloro palladium (24 mg, 0.03 mmol), and potassium acetate (294 mg, 3.00 mmol), 2-bromo-3,4,5,6-tetrahydro-azepino[5,4,3-cd]indol-6-one (239 mg, 0.90 mmol), a second portion of 1,1′-bis(diphenylphosphino)ferrocene dichloropalladium (24 mg, 0.03 mmol), and sodium carbonate (2.5 mL of a 2.0 M aqueous solution, 5.00 mmol) were reacted to yield 2-(4-hydroxy-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one, 39 mg (15%) as a beige solid: m.p. 300° C. (dec); 1H NMR (300 MHz, d6-DMSO) δ 3.00 (m, 2H), 3.37 (m, 2H), 6.92 (d, J=8.7 Hz, 2H), 7.16 (t, J=7.8 Hz, 1H), 7.49 (m, 3H), 7.65 (dd, J=7.5, 0.9 Hz, 1H), 8.04 (br t, 1H), 9.73 (br s, 1H), 11.40 (br s, 1H). MS (electrospray, MH+): 279. Anal. (C17H14N2O2) C, H, N.

Quelle

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