Lithium Carbonate → HCID 67389475, compound
Reaction equation
C1([C@]2(O)[CH2:8][CH2:7][NH:6][C@H:5]2[CH:9]([CH3:11])[CH3:10])CC1.[F:13][C:14]1[C:21]([CH3:22])=[C:20](F)[CH:19]=[CH:18][C:15]=1[C:16]#[N:17].[C:24](=[O:27])([O-])[O-].[Li+].[Li+]>>[F:13][C:14]1[C:21]([CH3:22])=[C:20]([N:6]2[CH2:5][C:9]([CH3:11])([CH3:10])[C@H:24]([OH:27])[C@H:7]2[CH3:8])[CH:19]=[CH:18][C:15]=1[C:16]#[N:17]Participants
4
Procedure
By an operation in the same manner as in Example 53 and using (2RS,3SR)-2,4,4-trimethylpyrrolidin-3-ol 0.5 oxalate (214 mg), 2,4-difluoro-3-methylbenzonitrile (240 mg) and lithium carbonate (246 mg), the title compound was obtained as a colorless solid (yield: 112 mg, yield: 35%).
Sources & evidence
- ORD record
- ord-7b8cb2d6715e4b8fbe74037aee664b11
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08013008B2
Reaction notes
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