Methyl iodide → HCID 16063636, compound
Reaction equation
[C:1]12(C3C(=O)NN(C4C=CC=CN=4)C=3C)CC3CC(CC(C3)C1)C2.IC.[C:26]12([C:36]3[C:37](=[O:49])[NH:38][N:39]([C:42]4[CH:47]=[CH:46][C:45]([F:48])=[CH:44][CH:43]=4)[C:40]=3[CH3:41])[CH2:35][CH:30]3[CH2:31][CH:32]([CH2:34][CH:28]([CH2:29]3)[CH2:27]1)[CH2:33]2>>[C:26]12([C:36]3[C:37](=[O:49])[N:38]([CH3:1])[N:39]([C:42]4[CH:43]=[CH:44][C:45]([F:48])=[CH:46][CH:47]=4)[C:40]=3[CH3:41])[CH2:33][CH:32]3[CH2:34][CH:28]([CH2:29][CH:30]([CH2:31]3)[CH2:35]1)[CH2:27]2Participants
4
Procedure
This compound was obtained in two steps in analogy to example 62 and 61 using 4-fluorophenylhydrazine (example 62) and using iodomethane and 4-adamantan-1-yl-1-(4-fluoro-phenyl)-5-methyl-1,2-dihydro-pyrazol-3-one (example 61) to give 4-adamantan-1-yl-1-(4-fluoro-phenyl)-2,5-dimethyl-1,2-dihydro-pyrazol-3-one as a yellow solid. MS (ESI+): 341.3 [M+H]+).
Sources & evidence
- ORD record
- ord-be05aa205d61487f821d0cbb0976b5dc
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07652057B2
Reaction notes
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