1-Morpholin-4-yl-cyclobutanecarbonitrile → C-(1-Morpholin-4-yl-cyclobutyl)-C-phenyl-methylamine
Reaction equation
[N:1]1([C:7]2([C:11]#[N:12])[CH2:10][CH2:9][CH2:8]2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[C:13]1([Li])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[N:1]1([C:7]2([CH:11]([NH2:12])[C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH2:10][CH2:9][CH2:8]2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1Participants
3
Procedure
The title compound, light yellow liquid, MS: m/e=247.3 [(M+H)+], was prepared in accordance with the general method of intermediate B from 1-morpholin-4-yl-cyclobutanecarbonitrile (intermediate T) and phenyllithium.
Sources & evidence
- ORD record
- ord-6636070661f246f0875247db5b5f3a70
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08063098B2
Reaction notes
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