Acetic Anhydride → HCID 18177412, compound
Reaction equation
[CH2:1]([O:6][C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[O:13][CH2:12][C:11]([CH2:17][NH2:18])=[CH:10]2)[CH2:2][CH2:3][CH2:4][CH3:5].[C:19](OC(=O)C)(=[O:21])[CH3:20]>N1C=CC=CC=1>[CH2:1]([O:6][C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[O:13][CH2:12][C:11]([CH2:17][NH:18][C:19](=[O:21])[CH3:20])=[CH:10]2)[CH2:2][CH2:3][CH2:4][CH3:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.34 g (1.38 mmol) of the amine obtained in Step F is acetylated with acetic anhydride in pyridine according to the usual procedure. The crude product of that reaction is purified on a silica column (eluant:ethyl acetate) to yield the title acetamide in the form of a white solid.
Workup
- customThe crude product of that reaction is purified on a silica column (eluant:ethyl acetate)
Sources & evidence
- ORD record
- ord-e34716af9be04819945c01236e1124f7
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06313160B1
Reaction notes
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