Cyclooctylamine → HCID 131729919, compound
Reaction equation
[Cl:1][C:2]1[N:11]=[C:10](Cl)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[CH:13]1([NH2:21])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.[CH3:22][C:23]1[CH:27]=[C:26]([CH3:28])[NH:25][N:24]=1>>[ClH:1].[CH:13]1([NH:21][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:24]3[C:23]([CH3:22])=[CH:27][C:26]([CH3:28])=[N:25]3)[N:11]=2)[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, cyclooctylamine and 3,5-dimethylpyrazole. Mp. 211° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-8b65e2b59f01417cad39bbd7cdceae8f
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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