Hydrogen chloride-ethyl acetate → HCID 69972355, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][N:11]([S:14]([CH3:17])(=[O:16])=[O:15])[CH2:10][C@@H:9]1[C:18]([OH:20])=[O:19])=O)(C)(C)C.[ClH:21].CCOC(C)=O>>[ClH:21].[CH3:17][S:14]([N:11]1[CH2:12][CH2:13][NH:8][C@@H:9]([C:18]([OH:20])=[O:19])[CH2:10]1)(=[O:15])=[O:16]Participants
3
Procedure
A solution of (2R)-1-tert-butoxycarbonyl-4-methanesulfonylpiperazine-2-carboxylic acid (2.90 g) in 4N HCl-AcOEt solution (40 ml) was stirred at room temperature for 30 minutes. The solution was concentrated in vacuo and the residue was solidified with Et2O to give 2.15 g of (2R)-4-methanesulfonylpiperazine-2-carboxylic acid hydrochloride as a powder.
Workup
- concentrationThe solution was concentrated in vacuo
Sources & evidence
- ORD record
- ord-224fa0b2374c4e7fb62691fd7e0675ba
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06333324B1
Reaction notes
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