Cyclopentylamine → 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([NH2:18])[CH2:17][CH2:16][CH2:15][CH2:14]1.[CH3:19][C:20]1[CH:24]=[C:23]([CH3:25])[NH:22][N:21]=1>>[ClH:1].[CH:13]1([NH:18][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:21]3[C:20]([CH3:19])=[CH:24][C:23]([CH3:25])=[N:22]3)[N:11]=2)[CH2:17][CH2:16][CH2:15][CH2:14]1Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, cyclopentylamine and 3,5-dimethylpyrazole Mp. 263.2° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-6c7228f89e9c467098d9a31db43e1749
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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