Iodoacetamide → HCID 14209997, compound
Reaction equation
[N:1]1([CH2:7]CCC2CCNCC2)[CH2:6]CCC[CH2:2]1.ICC(N)=O.N1(CCC[CH:30]2[CH2:35][CH2:34][N:33]([CH2:36][C:37]([NH2:39])=[O:38])[CH2:32][CH2:31]2)CCCCC1>>[CH3:2][N:1]([CH2:7][CH:32]1[CH2:31][CH2:30][CH2:35][CH2:34][N:33]1[CH2:36][C:37]([NH2:39])=[O:38])[CH3:6]Participants
4
Procedure
from 4-[3-(piperidin-1-yl)propyl]piperidine and iodoacetamide in a yield of 96% of theory, 2-[4-[3-(piperidin-1-yl)propyl]-piperidin-1-yl]acetamide, m.p. 94°-97° C.
Sources & evidence
- ORD record
- ord-6522ea731b204d739e359b5a5db2f3d1
- Source dataset
- uspto-grants-1989_10
- Patent number
- US04873236
Reaction notes
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