Lithium Carbonate → HCID 59273047, compound
Reaction equation
C1([C@:4]2([OH:12])[CH2:8][CH2:7][NH:6][C@H:5]2[CH:9](C)C)CC1.F[C:14]1[CH:21]=[CH:20][C:17]([C:18]#[N:19])=[C:16]([O:22][CH3:23])[CH:15]=1.[C:24](=O)([O-])[O-].[Li+].[Li+]>>[OH:12][C@H:4]1[CH2:8][C@@H:7]([CH3:24])[N:6]([C:14]2[CH:21]=[CH:20][C:17]([C:18]#[N:19])=[C:16]([O:22][CH3:23])[CH:15]=2)[C@H:5]1[CH3:9]Participants
4
Procedure
By an operation in the same manner as in Example 53 and using (2S,3S,5R)-2,5-dimethylpyrrolidin-3-ol 0.5 oxalate (62 mg), 4-fluoro-2-methoxybenzonitrile (70 mg) and lithium carbonate (63 mg), the title compound was obtained as a colorless solid (yield: 7 mg, yield: 7.3%).
Sources & evidence
- ORD record
- ord-a31e5470483649da89404f88c00bba6e
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08013008B2
Reaction notes
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