3,3-Difluoropiperidine hydrochloride → HCID 86683075, compound
Reaction equation
Cl[C:2]1[C:11]([C:12]2[NH:16][N:15]=[N:14][N:13]=2)=[C:10]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:9]2[C:4](=[CH:5][C:6]([F:24])=[C:7]([Cl:23])[CH:8]=2)[N:3]=1.Cl.[F:26][C:27]1([F:33])[CH2:32][CH2:31][CH2:30][NH:29][CH2:28]1>C(N(CC)CC)C>[Cl:23][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][C:6]=1[F:24])[N:3]=[C:2]([N:29]1[CH2:30][CH2:31][CH2:32][C:27]([F:33])([F:26])[CH2:28]1)[C:11]([C:12]1[N:16]=[N:15][NH:14][N:13]=1)=[C:10]2[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared in analogy to example 102 step C from 2,6-dichloro-7-fluoro-4-phenyl-3-(1H-tetrazol-5-yl)-quinoline (prepared as described in example 107 step B), 3,3-difluoro-piperidine hydrochloride and triethylamine. Off-white solid. MS (ESI): 445.4 (M+H)+.
Sources & evidence
- ORD record
- ord-a86e63f7965b427cb93f97b661d6e054
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09199938B2
Reaction notes
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