Hydrochloric Acid → HCID 24803422, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:33][C:11]3[C:12](=[O:32])[N:13]([C:16]4[CH:21]=[CH:20][C:19]([O:22][C@@H:23]5[CH2:28][CH2:27][CH2:26][N:25]([CH3:29])[CH2:24]5)=[C:18]([O:30][CH3:31])[CH:17]=4)[CH:14]=[CH:15][C:10]=3[CH:9]=2)=[CH:4][CH:3]=1.Cl>C(Cl)Cl.C(O)C>[ClH:1].[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:33][C:11]3[C:12](=[O:32])[N:13]([C:16]4[CH:21]=[CH:20][C:19]([O:22][C@@H:23]5[CH2:28][CH2:27][CH2:26][N:25]([CH3:29])[CH2:24]5)=[C:18]([O:30][CH3:31])[CH:17]=4)[CH:14]=[CH:15][C:10]=3[CH:9]=2)=[CH:4][CH:3]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Prepare the HCl salt by dissolving the residue in CH2Cl2 and adding HCl in ethanol. Add ether to the mixture then filter and dry the solid to obtain the title compound. LC-MS/ES m/z (35Cl) 481.0 [M+H]+.
Workup
- filtrationAdd ether to the mixture then filter
- customdry the solid
Sources & evidence
- ORD record
- ord-0d36d5d1b4f34819b40439dc3f29b0de
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263772B2
Reaction notes
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