Diethyl Ether → 1-Piperidineacetamide,4-[(4-fluorophenyl)methyl]-n-(3-nitrophenyl)-
Reaction equation
Cl[CH2:2][C:3]([NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=1)=[O:4].Cl.[F:16][C:17]1[CH:29]=[CH:28][C:20]([CH2:21]N2CCCCC2)=[CH:19][CH:18]=1.C(O[CH2:33][CH3:34])C>>[F:16][C:17]1[CH:18]=[CH:19][C:20]([CH2:21][CH:34]2[CH2:33][CH2:6][N:5]([CH2:2][C:3]([NH:5][C:6]3[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=3)=[O:4])[CH2:3][CH2:2]2)=[CH:28][CH:29]=1Participants
4
Procedure
The title compound is prepared from 2-chloro-N-(3-nitrophenyl)-acetamide and 4-(4-fluoro-benzyl-piperidine hydrochloride according to the method described in Example 142b. Melting Point: 118-120° C. (diethylether)
Sources & evidence
- ORD record
- ord-60935b6c69194d75ac8c89d566fe79f9
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435744B2
Reaction notes
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