Hydrochloric Acid → HCID 57445036, compound
Reaction equation
[N:1]1([CH2:7][CH2:8][CH2:9][N:10]2[CH2:15][CH2:14][N:13](C(OC(C)(C)C)=O)[CH2:12][C:11]2=[O:23])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[ClH:24]>C(OCC)(=O)C>[ClH:24].[N:1]1([CH2:7][CH2:8][CH2:9][N:10]2[CH2:15][CH2:14][NH:13][CH2:12][C:11]2=[O:23])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Through a solution of tert-butyl 4-(3-morpholin-4-ylpropyl)-3-oxopiperazine-1-carboxylate (45 mg, 0.14 mmol) in 5 mL of ethyl acetate at 0° C. was bubbled HCl gas for 2 minutes. After stirring an additional 30 minutes, the reaction was concentrated in vacuo to provide the titled product. ESI+MS: 228.4 [M+H]+.
Workup
- concentrationthe reaction was concentrated in vacuo
Sources & evidence
- ORD record
- ord-f1b7a322c41142e896dfe8e9871f4ee3
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07560546B2
Reaction notes
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