4-Fluoroaniline → 1-(4-fluorophenyl)-7-methyl-1H-[1,2,3]triazolo[4,5-c]pyridine
Reaction equation
Cl[C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][N:5]=[CH:4][C:3]=1[CH3:11].ClC1C=C[N:16]=CC=1[N+]([O-])=O.[F:22][C:23]1[CH:29]=[CH:28][C:26]([NH2:27])=[CH:25][CH:24]=1.NC1C=CC=CN=1>>[F:22][C:23]1[CH:29]=[CH:28][C:26]([N:27]2[C:2]3[C:3]([CH3:11])=[CH:4][N:5]=[CH:6][C:7]=3[N:8]=[N:16]2)=[CH:25][CH:24]=1Participants
5
Procedure
The title compound was prepared in a manner analogous to Intermediate 17, Step 1 through Intermediate 19, Step 3 substituting 4-chloro-3-methyl-5-nitro-pyridine for 4-chloro-3-nitropyridine and 4-fluoroaniline for 2-aminopyridine in the synthesis of Intermediate 17, Step 1. MS (ESI) mass calcd. C12H9FN4, 228.1. m/z found, 229.1 [M+H]+.
Sources & evidence
- ORD record
- ord-64d4e4e8d90f4377ba776133b40a2492
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09066946B2
Reaction notes
Loading…