5-(5-Nitro-benzofuran-7-yl)-pyridin-2-ylamine → 5-(5-Amino-1-benzofuran-7-yl)pyridin-2-amine
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([C:13]2[CH:14]=[CH:15][C:16]([NH2:19])=[N:17][CH:18]=2)[C:7]2[O:11][CH:10]=[CH:9][C:8]=2[CH:12]=1)([O-])=O.N1(CCNC2C3OC=CC=3C=C(N)C=2)CCOCC1>>[NH2:1][C:4]1[CH:5]=[C:6]([C:13]2[CH:14]=[CH:15][C:16]([NH2:19])=[N:17][CH:18]=2)[C:7]2[O:11][CH:10]=[CH:9][C:8]=2[CH:12]=1Participants
3
Procedure
The title compound was prepared from 5-(5-nitro-benzofuran-7-yl)-pyridin-2-ylamine (Intermediate 39) according to the procedure of Intermediate 28. The product was used directly in the subsequent reaction.
Workup
- customThe product was used directly in the subsequent reaction
Sources & evidence
- ORD record
- ord-4279f1efc3e244cfb626bea9d318ac03
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07820675B2
Reaction notes
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