Hydrochloric Acid → HCID 54372821, compound
Reaction equation
C([O:5][C:6](=[O:36])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([C@H:15]([N:22]([C:24](=[O:35])[CH2:25][C:26]2[C:30]3[CH:31]=[CH:32][CH:33]=[CH:34][C:29]=3[O:28][CH:27]=2)[CH3:23])[CH2:16][N:17]2[CH2:21][CH2:20][CH2:19][CH2:18]2)[CH:10]=1)(C)(C)C.Cl>ClCCl>[O:28]1[C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=2[C:26]([CH2:25][C:24]([N:22]([CH3:23])[C@@H:15]([C:11]2[CH:10]=[C:9]([CH:14]=[CH:13][CH:12]=2)[O:8][CH2:7][C:6]([OH:36])=[O:5])[CH2:16][N:17]2[CH2:21][CH2:20][CH2:19][CH2:18]2)=[O:35])=[CH:27]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of Example 18 (1.272 g, 2.58 mmol) in dichloromethane (10 mL) was added HCl (2.5 mL of 4 M solution in dioxan). After stirring for 24 hours, all volatiles were removed in vacuo and the resulting solid washed with acetonitrile. After removing the solvent, the resulting solid was dried to give a beige solid, 0.50 g.
Workup
- customall volatiles were removed in vacuo
- washthe resulting solid washed with acetonitrile
- customAfter removing the solvent
- customthe resulting solid was dried
- customto give a beige solid, 0.50 g
Sources & evidence
- ORD record
- ord-150a43c1fd8b476b810454cd3604e098
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06057357
Reaction notes
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