4-Chloropyridine hydrochloride → (2-Methyl-indol-1-yl)-pyridin-4-yl-amine
Reaction equation
[CH3:1][C:2]1[N:3]([NH2:11])[C:4]2[C:9]([CH:10]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2.Cl.Cl[C:14]1[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=1>>[CH3:1][C:2]1[N:3]([NH:11][C:14]2[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=2)[C:4]2[C:9]([CH:10]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2Participants
3
Procedure
The title compound was prepared from 2-methyl-1H-indol-1-amine and 4-chloropyridine hydrochloride at 120° C. for 30 minutes in substantially the same manner as in Example 1, m.p. 75°-78° C.
Sources & evidence
- ORD record
- ord-8290763803c94dbdbb2ad8ad139937d8
- Source dataset
- uspto-grants-1991_08
- Patent number
- US05039811
Reaction notes
Loading…