2-ethyl-2H-tetrazol-5-amine → HCID 9858931, compound
Reaction equation
[NH2:1][C:2]1[N:3]=[N:4][N:5]([CH2:7][CH3:8])[N:6]=1.[CH:9]1[C:19]2[CH:18]([C:20](Cl)=[O:21])[C:17]3[CH:23]=[CH:24][CH:25]=[CH:26][C:16]=3[CH2:15][O:14][C:13]=2[CH:12]=[CH:11][CH:10]=1>>[CH2:7]([N:5]1[N:4]=[N:3][C:2]([NH:1][C:20]([CH:18]2[C:17]3[CH:23]=[CH:24][CH:25]=[CH:26][C:16]=3[CH2:15][O:14][C:13]3[CH:12]=[CH:11][CH:10]=[CH:9][C:19]2=3)=[O:21])=[N:6]1)[CH3:8]Participants
3
Procedure
The title compound, yellow solid, m.p. 158-159° and MS: (neg. ions): m/e=334.1 (M+−H) was prepared in accordance with the general method of example 1 from 5-amino-2-ethyl-2H-tetrazole and 6,11 -dihydro-dibenzo[b,e]oxepine-11-carbonyl chloride.
Sources & evidence
- ORD record
- ord-f0caf63213f24c36a7044852cad38e90
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06399641B1
Reaction notes
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