Triethylamine → HCID 57876318, compound
Reaction equation
Br[CH2:2][N:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1.Cl.[Cl:10][C:11]1[CH:16]=[CH:15][C:14]([NH:17]N)=[CH:13][C:12]=1[F:19].[CH3:20][N:21]1[CH2:26][CH2:25][C:24](=O)[CH2:23][CH2:22]1.[CH2:28](N(CC)CC)C>>[Cl:10][C:11]1[C:12]([F:19])=[CH:13][C:14]2[N:17]([CH2:28][CH2:2][N:3]3[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]3)[C:24]3[CH2:23][CH2:22][N:21]([CH3:20])[CH2:26][C:25]=3[C:15]=2[CH:16]=1Participants
5
Procedure
The title compound is prepared by following General Method 8 by using 1-(bromomethyl)piperidine, 4-chloro-3-fluorophenylhydrazine hydrochloride, triethylamine and N-methyl-4-piperidone.
Sources & evidence
- ORD record
- ord-210bde6975ac4882b0eee0084d735a2b
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09034880B2
Reaction notes
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