Phenyl chloroformate → HCID 70089498, compound
Reaction equation
[C:1]1([C:7]2[N:22]=[C:10]3[CH:11]=[C:12]([C:16]4[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=4)[CH:13]=[C:14]([NH2:15])[N:9]3[N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl[C:24]([O:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)=[O:25]>>[C:27]1([O:26][C:24](=[O:25])[NH:15][C:14]2[N:9]3[N:8]=[C:7]([C:1]4[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=4)[N:22]=[C:10]3[CH:11]=[C:12]([C:16]3[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=3)[CH:13]=2)[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1Participants
3
Procedure
The title compound, MS m/e (%): 408 (M+H+, 100), was prepared in accordance with the general method of example 31 from 2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine and phenyl chloroformate.
Sources & evidence
- ORD record
- ord-8cc6d93c7f8c4897aaac81b051b6582f
- Source dataset
- uspto-grants-2002_03
- Patent number
- US06355653B1
Reaction notes
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