Hydrochloric Acid → HCID 131717974, compound
Reaction equation
CC(C)(OC([NH:7][C@H:8]([C:13]([NH:15][CH:16]([CH2:25][CH:26]1[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1)[CH:17]([P:19]([O:23][CH3:24])([O:21][CH3:22])=[O:20])[OH:18])=[O:14])[CH2:9][CH:10]([CH3:12])[CH3:11])=O)C.[ClH:33]>C(OCC)(=O)C>[ClH:33].[CH:26]1([CH2:25][C@H:16]([NH:15][C:13](=[O:14])[C@H:8]([CH2:9][CH:10]([CH3:11])[CH3:12])[NH2:7])[CH:17]([P:19]([O:23][CH3:24])([O:21][CH3:22])=[O:20])[OH:18])[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound of Example 1 (2.29 g, 4.8 mmol) was dissolved in a 1.2N solution of hydrochloric acid in ethyl acetate (25 mL). After 1 hour, the reaction mixture was concentrated yielding 2.2 g of the title A compound.
Workup
- concentrationthe reaction mixture was concentrated
- customyielding 2.2 g of the title A compound
Sources & evidence
- ORD record
- ord-f0782f004d69450fa0cdfb1145e6fb5a
- Source dataset
- uspto-grants-1993_06
- Patent number
- US05217958
Reaction notes
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