Hydrogen chloride-ethyl acetate → HCID 69749936, compound
Reaction equation
[ClH:1].C(OCC)(=O)C.C(OC([N:15]1[CH2:20][CH2:19][N:18]([C:21](=[O:55])[C@@H:22]([NH:30][C:31]([CH2:33][N:34]2[C:39]([C:40]3[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=3)=[CH:38][N:37]([C:46](=[O:50])[CH2:47][O:48][CH3:49])[CH:36]([CH:51]([CH3:53])[CH3:52])[C:35]2=[O:54])=[O:32])[CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH2:17][CH2:16]1)=O)(C)(C)C>C(OCC)(=O)C>[ClH:1].[CH:51]([CH:36]1[N:37]([C:46](=[O:50])[CH2:47][O:48][CH3:49])[CH:38]=[C:39]([C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=2)[N:34]([CH2:33][C:31]([NH:30][C@@H:22]([CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[C:21](=[O:55])[N:18]2[CH2:19][CH2:20][NH:15][CH2:16][CH2:17]2)=[O:32])[C:35]1=[O:54])([CH3:53])[CH3:52]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 4 N hydrogen chloride/ethyl acetate solution (0.24 ml) is added to a solution of (2S)-1-(4-tert-butoxycarbonylpiperazin-1-yl)-2-{(3RS)-3-isopropyl-4-methoxyacetyl-2-oxo-6-phenyl-1,2,3,4-tetrahydropyrazin-1-yl}methylcarbonylamino-1-oxo-3-phenylpropane (190 mg, Compound No. 1-55) in ethyl acetate (3 ml), and the mixture is stirred for one hour. The reaction mixture is concentrated under reduced pressure to give the titled compound (146 mg).
Workup
- concentrationThe reaction mixture is concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-d506b005055b42b8b82ce696237d278b
- Source dataset
- uspto-grants-2005_11
- Patent number
- US06960575B2
Reaction notes
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