Acetic Anhydride → HCID 14371425, compound
Reaction equation
[CH3:1][CH:2]([N:4]([CH:23]([CH3:25])[CH3:24])[CH2:5][CH2:6][C:7]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)([CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][NH:12]1)[C:8]([NH2:10])=[O:9])[CH3:3].[C:26](OC(=O)C)(=[O:28])[CH3:27]>>[C:26]([N:12]1[CH2:13][CH2:14][CH2:15][CH2:16][CH:11]1[C:7]([CH2:6][CH2:5][N:4]([CH:2]([CH3:1])[CH3:3])[CH:23]([CH3:25])[CH3:24])([C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1)[C:8]([NH2:10])=[O:9])(=[O:28])[CH3:27]Participants
3
Procedure
acylating α-[2-[bis(1-methylethyl)amino]ethyl]-α-phenyl-2-piperidineacetamide with acetic anhydride to form 1-acetyl-α-[2-[bis(1-methylethyl)amino]ethyl]-α-phenyl-2-piperidineacetamide;
Sources & evidence
- ORD record
- ord-4314ab3989d1460ba79056b1933b20e5
- Source dataset
- uspto-grants-1988_12
- Patent number
- US04791199
Reaction notes
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