1-Benzyl-1H-[1,2,4]triazol-3-ylamine → HCID 46216252, compound
Reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]([N:10]2[CH:14]=[C:13]([CH3:15])[N:12]=[CH:11]2)=[C:6]([CH:9]=1)[C:7]#[N:8].[CH2:16]([N:23]1[CH:27]=[N:26][C:25]([NH2:28])=[N:24]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[CH2:16]([N:23]1[CH:27]=[N:26][C:25]([NH:28][C:2]2[CH:3]=[CH:4][C:5]([N:10]3[CH:14]=[C:13]([CH3:15])[N:12]=[CH:11]3)=[C:6]([CH:9]=2)[C:7]#[N:8])=[N:24]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1Participants
3
Procedure
Prepared in analogy to example 1b) starting with 5-bromo-2-(4-methyl-imidazol-1-yl)-benzonitrile and 1-benzyl-1H-[1,2,4]triazol-3-ylamine. The title compound was obtained as a white solid (Yield=25%). MS ISP (m/e): 356.1 (100) [(M+H)+].
Workup
- customPrepared in analogy to example 1b)
Sources & evidence
- ORD record
- ord-4bed3084d00841c58f38325ec3c68f67
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288403B2
Reaction notes
Loading…