1,2,3,6-Tetrahydropyridine → 4-(3,6-dihydro-2H-pyridin-1-yl)naphthalene-1-carbonitrile
Reaction equation
[C:1]([C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6](F)=[CH:5][CH:4]=1)#[N:2].[NH:14]1[CH2:19][CH:18]=[CH:17][CH2:16][CH2:15]1>>[N:14]1([C:6]2[C:7]3[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=3)[C:3]([C:1]#[N:2])=[CH:4][CH:5]=2)[CH2:15][CH:16]=[CH:17][CH2:18][CH2:19]1Participants
3
Procedure
The title compound (7 mg, 26% yield) was prepared as described for 196MBT2-4 from 1-cyano-4-fluoronaphthalene (20 mg, 0.117 mmol) and 1,2,3,6-tetrahydropyridine (39 mg, 0.468 mmol).
Sources & evidence
- ORD record
- ord-0194ff9666d74041880720a6a098a601
- Source dataset
- uspto-grants-2007_09
- Patent number
- US07268232B2
Reaction notes
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