1-((2,4-Dichlorophenyl)methyl)-1H-pyrazol-3-amine → [1-(2,4-Dichloro-benzyl)-1H-pyrazol-3-yl]-[1-(3-methyl-[1,2,4]thiadiazol-5-yl)-piperidin-4-yl]-amine
Reaction equation
[CH3:1][C:2]1[N:6]=[C:5]([N:7]2[CH2:12][CH2:11][C:10](=O)[CH2:9][CH2:8]2)[S:4][N:3]=1.[Cl:14][C:15]1[CH:27]=[C:26]([Cl:28])[CH:25]=[CH:24][C:16]=1[CH2:17][N:18]1[CH:22]=[CH:21][C:20]([NH2:23])=[N:19]1>>[Cl:14][C:15]1[CH:27]=[C:26]([Cl:28])[CH:25]=[CH:24][C:16]=1[CH2:17][N:18]1[CH:22]=[CH:21][C:20]([NH:23][CH:10]2[CH2:11][CH2:12][N:7]([C:5]3[S:4][N:3]=[C:2]([CH3:1])[N:6]=3)[CH2:8][CH2:9]2)=[N:19]1Participants
3
Procedure
Prepared in analogy to example 1 step h) starting from 1-(3-methyl-[1,2,4]thiadiazol-5-yl)-piperidin-4-one (example 1c) and 1-(2,4-dichloro-benzyl)-1H-pyrazol-3-ylamine. The title compound was obtained as a colorless oil (yield=56%).
Workup
- customPrepared in analogy to example 1 step h)
Sources & evidence
- ORD record
- ord-0e95c66d07824572a5969d70c2e3b0c6
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08486967B2
Reaction notes
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