2,2-Diethoxyethylamine → HCID 18943443, compound
Reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11](=O)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:15]([O:17][CH:18]([O:21][CH2:22][CH3:23])[CH2:19][NH2:20])[CH3:16]>>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([NH:20][CH2:19][CH:18]([O:21][CH2:22][CH3:23])[O:17][CH2:15][CH3:16])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
The N-(1-tert-butyloxycarbonyl-4-piperidinyl)-N-(2,2-di-ethoxyethyl)amine [Rf : 0.48 (reversed phase silica gel; methanol/5% aqueous brine=6:4)] employed is prepared by reductive amination of 1-tert-butyloxycarbonyl-4-piperidone with aminoacetaldehyde diethyl acetal
Sources & evidence
- ORD record
- ord-ba2225c8df2545d0bd2e72a772527e62
- Source dataset
- uspto-grants-1998_10
- Patent number
- US05827849
Reaction notes
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