3-Pyridineacetonitrile → tert-Butyl 4-cyano-4-(pyridin-3-yl)piperidine-1-carboxylate
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]#[N:9])[CH:2]=1.Cl[CH2:11][CH2:12][N:13]([CH2:21][CH2:22]Cl)[C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15]>>[C:17]([O:16][C:14]([N:13]1[CH2:21][CH2:22][C:7]([C:8]#[N:9])([C:3]2[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=2)[CH2:11][CH2:12]1)=[O:15])([CH3:20])([CH3:19])[CH3:18]Participants
3
Procedure
Prepare by the method of example 30.2 using 3-pyridylacetonitrile (10 mmol) and 2-chloro-N-(2-chloroethyl)-N-tert-butoxycarbonyl-ethanamine (11 mmol).
Sources & evidence
- ORD record
- ord-4f2b25ac94824791a82b8635a8f96cde
- Source dataset
- uspto-grants-1997_06
- Patent number
- US05635510
Reaction notes
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