Hydrochloric Acid → HCID 178525209, compound
Reaction equation
[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[NH:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][NH:16][C:17](=[O:39])[CH2:18][N:19]1[CH2:25][CH2:24][CH:23]([CH2:26][C:27]([O:29]C(C)(C)C)=[O:28])[C:22]2[CH:34]=[CH:35][CH:36]=[CH:37][C:21]=2[C:20]1=[O:38].[ClH:40]>C(O)(=O)C.O1CCOCC1.O>[Cl-:40].[C:27]([CH2:26][CH:23]1[C:22]2[CH:34]=[CH:35][CH:36]=[CH:37][C:21]=2[C:20](=[O:38])[N:19]([CH2:18][C:17]([NH:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][NH:10][C:2]2[NH2+:3][C:4]3[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=3[N:1]=2)=[O:39])[CH2:25][CH2:24]1)([OH:29])=[O:28]Participants
6
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
Analagously to Example II, the tert-butyl ester (Example XIII) in glacial acetic acid was cleaved using 4N HCl in dioxane. After stripping off the solvent, the residue was dissolved in water, clarified using active carbon and then lyophilized; 0.67 g of white amorphous residue; ESI-MS [M+H+]: 478.
Sources & evidence
- ORD record
- ord-74b4677fc8cc4a53b4a57c499ba33fab
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07279468B2
Reaction notes
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