Hydrochloric Acid → HCID 21188383, compound
Reaction equation
[C:1]([CH2:4][O:5][CH2:6][CH2:7][N:8]1[CH2:13][CH2:12][N:11](C(OC(C)(C)C)=O)[CH2:10][CH2:9]1)(=[O:3])[NH2:2].[ClH:21].O>C(OCC)(=O)C>[ClH:21].[ClH:21].[N:8]1([CH2:7][CH2:6][O:5][CH2:4][C:1]([NH2:2])=[O:3])[CH2:9][CH2:10][NH:11][CH2:12][CH2:13]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1.4 g (0.005 mol) of tert-butyl 4-(2-carbamoylmethoxyethyl)piperazine-1-carboxylate prepared in Example I.4.1. and 14 ml of a 3M solution of hydrochloric acid in ethyl acetate are introduced into a 50 ml three-necked round-bottomed flask fitted with a water-cooled condenser and a mechanical stirrer. The mixture is stirred at room temperature for 2 hours. The precipitate is filtered off and is washed with ethyl acetate. 1.3 g (100%) of 2-(1-piperazinyl)ethoxyacetamide dihydrochloride are obtained.
Workup
- temperaturecooled condenser and a mechanical stirrer
- filtrationThe precipitate is filtered off
- washis washed with ethyl acetate
Sources & evidence
- ORD record
- ord-ebfefd78592745d99838c023a42c434e
- Source dataset
- uspto-grants-2000_10
- Patent number
- US06140501
Reaction notes
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