تفاعل #587201

ord-e8e694d3ff8b4fc4a4890bf8c1a21a9d

معادلة التفاعل

Oc1cccc2c1CCN2c1ccc(I)cc1
1-(4-iodophenyl)indolin-4-ol
O=[N+]([O-])c1ccc(F)cc1
1-fluoro-4-nitrobenzene
COc1cccc2[nH]ccc12
4-methoxy-1H-indole
O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
COc1cccc2c1ccn2-c1ccc([N+](=O)[O-])cc1
4-methoxy-1-(4-nitrophenyl)-1H-indole

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىis provided in Reaction Scheme 4b

الإجراء التجريبي

The synthesis of 1-(4-iodophenyl)indolin-4-ol (92) is provided in Reaction Scheme 4b. The reaction of 1-fluoro-4-nitrobenzene and 4-methoxy-1H-indole in the presence of Cs2CO3 gave 4-methoxy-1-(4-nitrophenyl)-1H-indole (88), which was reduced with H2/Pd to yield 4-(4-methoxy-1H-indol-1-yl)benzenamine (89). The amino group of 89 was converted via the Sandmeyer reaction to 1-(4-iodophenyl)-4-methoxy-1H-indole (90) which on reduction with sodium borocyanohyride gave 1-(4-iodophenyl)-4-methoxyindoline (91). The indoline 91 was demethylated with BBr3 to provide the desired 92.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07767834B2uspto-grants-2010_08