Bromoacetonitrile → 4-[2-[(Diethylamino)methyl]-piperidin-1-yl]butane nitrile
Reaction equation
[CH2:1]([N:4]([CH2:8][CH:9]1[CH2:14][CH2:13][CH2:12][CH2:11][NH:10]1)[CH2:5][CH2:6]C)[CH2:2]C.BrCC#N.C([N:22]([CH2:26][CH:27]1[CH2:32][CH2:31]CCN1CC#N)CCC)CC>ClCCl.C(OCC)(=O)C>[CH2:1]([N:4]([CH2:8][CH:9]1[CH2:14][CH2:13][CH2:12][CH2:11][N:10]1[CH2:31][CH2:32][CH2:27][C:26]#[N:22])[CH2:5][CH3:6])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
from 2-[(dipropylamino)methyl]piperidine and 2-bromoacetonitrile, (±)-2-[2-[(dipropylamino)methyl]piperidin-1-yl]acetonitrile, RF 0.9 (Macherey-Nagel, PolygramRSIL G/UV254, pre-coated plastic sheets for TLC, eluant: dichloromethane/ethyl acetate 50:50 v/v).
Sources & evidence
- ORD record
- ord-86fbff9b1c5a4f72bcb9803d828abca4
- Source dataset
- uspto-grants-1989_10
- Patent number
- US04873236
Reaction notes
Loading…