Butylamine → HCID 54389479, compound
Reaction equation
[CH:1]1([O:7][N:8]2[C:13]([CH3:15])([CH3:14])[CH2:12][C:11](=O)[CH2:10][C:9]2([CH3:18])[CH3:17])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:19]([NH2:23])[CH2:20][CH2:21][CH3:22]>>[CH:1]1([O:7][N:8]2[C:13]([CH3:15])([CH3:14])[CH2:12][CH:11]([CH2:22][CH2:21][CH2:20][CH2:19][NH2:23])[CH2:10][C:9]2([CH3:18])[CH3:17])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
3
Procedure
The product is prepared analogously to the method described in Example II-1, by reaction of 126.7 g (0.5 moles) of 1-cyclohexyloxy-2,2,6,6-tetramethyl-4-oxopiperidine and 38.4 g (0.52 moles) of n-butylamine.
Workup
- customThe product is prepared analogously to the method
Sources & evidence
- ORD record
- ord-67b27bb5c1524e7484ed64423cfc2764
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06265473B1
Reaction notes
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