HCID 11391453, compound → HCID 66842237, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[CH:9]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH2:10][C:11](=O)[CH:12]([CH3:14])[CH3:13])=[CH:4][CH:3]=1.[CH2:23]([O:30][CH:31]1[CH2:36][CH:35]([O:37][CH3:38])[O:34][CH:33]([CH2:39][CH2:40][NH2:41])[CH2:32]1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[CH2:23]([O:30][CH:31]1[CH2:36][CH:35]([O:37][CH3:38])[O:34][CH:33]([CH2:39][CH2:40][N:41]2[C:11]([CH:12]([CH3:14])[CH3:13])=[CH:10][C:9]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[C:8]2[C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)[CH2:32]1)[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1Participants
3
Procedure
According to the same method as in Example 4-1, the title compound was synthesized using 1-(4-fluorophenyl)-5-methyl-2-phenyl-1,4-hexanedione and 2-(4-(benzyloxy)-6-methoxytetrahydro-2H-pyran-2-yl)ethanamine.
Sources & evidence
- ORD record
- ord-ded32958fcc843cc95a1334e6ae62b0a
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08178697B2
Reaction notes
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