Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][N:8]=2)[CH:3]=[CH:2]1.[CH3:10]C1C2C(=CC=CC=2)NC=1>>[CH3:10][N:1]1[C:9]2=[N:8][CH:7]=[CH:6][CH:5]=[C:4]2[CH:3]=[CH:2]1Participants
3
Procedure
According to the procedure of Preparation 40(a), except substituting 7-azaindole (2.28 g, 1.83 mmole) for the 3-methylindole, the title compound (1.4 g, 58%) was prepared as a yellow oil: MS (ES) m/e 133 (M+H)+.
Sources & evidence
- ORD record
- ord-91ad8c52c923465bb6c8f6d690e8f927
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557125B2
Linked notes
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