Lithium Carbonate → HCID 59273024, compound

HRID 907023Notes

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)[CH2:3]C1.[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]([CH2:1][CH3:3])([OH:12])[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

Reactant 3

HCID 11125Lithium Carbonate

HCID 7371772,4,6-Trifluorobenzonitrile

HCID 59273011(2S,3R)-3-cyclopropyl-2-isopropylpyrrolidin-3-ol

Product 1

HCID 59273024HCID 59273024, compound

Procedure

By an operation in the same manner as in Example 1 and using (2S,3S)-2,3-diethylpyrrolidin-3-ol 0.5 oxalate (197 mg), 2,4,6-trifluorobenzonitrile (295 mg) and lithium carbonate (192 mg), the title compound was obtained as a colorless solid (yield: 157 mg, yield: 54%).

Sources & evidence

ORD record: ord-a651e74ab0c64026b119b258a8fc198b
Source dataset: uspto-grants-2011_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08013008B2

Reaction notes

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