Lithium Carbonate → HCID 59273076, compound
Reaction equation
[CH:1]1([C@:4]2([OH:12])[CH2:8][CH2:7][NH:6][C@H:5]2[CH:9]([CH3:11])C)CC1.[F:13][C:14]1[CH:21]=[C:20](F)[CH:19]=[C:18]([F:23])[C:15]=1[C:16]#[N:17].C(=O)([O-])[O-].[Li+].[Li+]>>[CH2:9]([C@H:5]1[C@:4]([OH:12])([CH3:1])[CH2:8][CH2:7][N:6]1[C:20]1[CH:21]=[C:14]([F:13])[C:15]([C:16]#[N:17])=[C:18]([F:23])[CH:19]=1)[CH3:11]Participants
4
Procedure
By an operation in the same manner as in Example 1 and using (2S,3S)-2-ethyl-3-methylpyrrolidin-3-ol 0.5 oxalate (200 mg), 2,4,6-trifluorobenzonitrile (270 mg) and lithium carbonate (187 mg), the title compound was obtained as a colorless solid (yield: 187.5 mg, yield: 61%).
Sources & evidence
- ORD record
- ord-d0354e58a83b499e939eabdb6ac86b89
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08013008B2
Reaction notes
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