4-Methylcyclohexylamine → HCID 131729927, 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.[CH3:13][CH:14]1[CH2:19][CH2:18][CH:17]([NH2:20])[CH2:16][CH2:15]1.[CH:21]([C:24]1[CH:28]=[C:27]([CH:29]([CH3:31])[CH3:30])[NH:26][N:25]=1)([CH3:23])[CH3:22]>>[ClH:1].[CH:21]([C:24]1[CH:28]=[C:27]([CH:29]([CH3:31])[CH3:30])[N:26]([C:2]2[N:11]=[C:10]([NH:20][CH:17]3[CH2:18][CH2:19][CH:14]([CH3:13])[CH2:15][CH2:16]3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:25]=1)([CH3:23])[CH3:22]Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, 4-methylcyclohexylamine and 3,5-diisopropylpyrazole. Mp. 134.6° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-4d671d7da0844f6fb8e28c4f888af109
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
Loading…