Cycloheptylamine → HCID 131729917, 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([NH2:20])[CH2:19][CH2:18][CH2:17][CH2:16]CC1.[CH3:21][C:22]1[CH:26]=[C:25]([CH3:27])[NH:24][N:23]=1>>[ClH:1].[CH:13]1([NH:20][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:23]3[C:22]([CH3:21])=[CH:26][C:25]([CH3:27])=[N:24]3)[N:11]=2)[CH2:16][CH2:17][CH2:18][CH2:19]1Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, cycloheptylamine and 3,5-dimethylpyrazole. Mp. 207° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-a451d1b49684492e8d78ff5045232af9
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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