Hydrochloric Acid → HCID 86696474, compound
Reaction equation
[ClH:1].[CH3:2][CH:3]1[CH2:8][N:7](C(OC(C)(C)C)=O)[CH2:6][CH2:5][N:4]1[C:16]([O:18][CH:19]([CH3:21])[CH3:20])=[O:17]>CO>[ClH:1].[CH3:2][CH:3]1[CH2:8][NH:7][CH2:6][CH2:5][N:4]1[C:16]([O:18][CH:19]([CH3:21])[CH3:20])=[O:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Concentrated hydrochloric acid (6.0 mL) was added to a solution of 4-tert-butyl 1-isopropyl 2-methylpiperazine-1,4-dicarboxylate (4.2 g, 14.6 mmol) in methanol (250 mL) and allowed to stir at ambient temperature under N2 blanket for 3d. The solution was then evaporated to dryness and the resultant viscous yellow oil triturated in acetone to precipitate a fine white powder which was isolated by filtration, under N2 blanket, to afford 2.0 g. LRMS (ESI) m/z 187.0 [(M+H)]+, calc'd for C9H18N2O2: 186.26.
Workup
- customThe solution was then evaporated to dryness
- customthe resultant viscous yellow oil triturated in acetone
- customto precipitate a fine white powder which
- customwas isolated by filtration, under N2 blanket
- customto afford 2.0 g
Sources & evidence
- ORD record
- ord-0a96ba208f00428c9fff8b8fd45ab4df
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08969565B2
Reaction notes
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