Hydrochloric Acid → HCID 131719082, compound
Reaction equation
[Cl:1][C:2]1[CH:30]=[CH:29][C:5]2[O:6][C:7]3[CH:28]=[CH:27][CH:26]=[CH:25][C:8]=3[CH2:9][N:10]([C:11]([NH:13][CH2:14][C:15]([NH:17][CH2:18][C:19]3[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=3)=[O:16])=[O:12])[C:4]=2[CH:3]=1.Cl.CO>O>[ClH:1].[Cl:1][C:2]1[CH:30]=[CH:29][C:5]2[O:6][C:7]3[CH:28]=[CH:27][CH:26]=[CH:25][C:8]=3[CH2:9][N:10]([C:11]([NH:13][CH2:14][C:15]([NH:17][CH2:18][C:19]3[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=3)=[O:16])=[O:12])[C:4]=2[CH:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To the title compound of Example 5 (0.10 g, 0.23 mmol) suspended in 30 mL of water was added 0.5 mL of 1N HCl. After stirring this suspension overnight at room temperature, 15 mL of MeOH were added giving a homogeneous solution. This reaction was diluted to 100 mL with water and lyophilized to provide 92 mg of the title compound as a white solid salt.
Workup
- customgiving a homogeneous solution
Sources & evidence
- ORD record
- ord-f2e11b2c572f478c9b759f5cb5a7c4d8
- Source dataset
- uspto-grants-1997_08
- Patent number
- US05661146
Reaction notes
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