Hydrogen Bromide → HCID 376124, compound
Reaction equation
C(OC([NH:11][CH2:12][C:13]([NH:15][C:16]1[CH:29]=[CH:28][CH:27]=[CH:26][C:17]=1[C:18]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:19])=[O:14])=O)C1C=CC=CC=1.[BrH:30].CCOCC>C(O)(=O)C>[BrH:30].[NH2:11][CH2:12][C:13]([NH:15][C:16]1[CH:29]=[CH:28][CH:27]=[CH:26][C:17]=1[C:18]([C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)=[O:19])=[O:14]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of N-benzyloxycarbonyl derivative (2a, 3.13 g, 8.06 mmol) obtained in Preparation 1 and a solution of 30% hydrobromic acid in acetic acid is stirred for 1 hour. Excess ether is added, and the resultant precipitate is filtered off. After washing with ether, it is dried to obtain 2.50 g (92%) of hydrobromate (compound 3a).
Workup
- customobtained in Preparation 1
- filtrationthe resultant precipitate is filtered off
- washAfter washing with ether, it
- customis dried
Sources & evidence
- ORD record
- ord-6d57f4745829462e90f9b08758c91d70
- Source dataset
- uspto-grants-1998_04
- Patent number
- US05739162
Reaction notes
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