Hydrochloric Acid → HCID 70298437, compound
Reaction equation
C([O:5][C:6](=[O:37])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH:15]([N:23]([C:25](=[O:36])[CH2:26][C:27]2[O:28][C:29]3[CH:35]=[CH:34][CH:33]=[CH:32][C:30]=3[CH:31]=2)[CH3:24])[CH2:16][N:17]2[CH2:21][CH2:20][CH:19]([OH:22])[CH2:18]2)[CH:10]=1)(C)(C)C.Cl>ClCCl>[O:28]1[C:29]2[CH:35]=[CH:34][CH:33]=[CH:32][C:30]=2[CH:31]=[C:27]1[CH2:26][C:25]([N:23]([CH3:24])[CH:15]([C:11]1[CH:10]=[C:9]([CH:14]=[CH:13][CH:12]=1)[O:8][CH2:7][C:6]([OH:37])=[O:5])[CH2:16][N:17]1[CH2:21][CH2:20][CH:19]([OH:22])[CH2:18]1)=[O:36]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of Example 32 (0.824 g, 1.62 mmol) in dichloromethane (15 mL) was added HCl (3 mL of 4 M solution in dioxan). After stirring for 22 hours, all volatiles were removed in vacuo, and the resulting solid was washed with ethyl acetate (twice). The remaining solid was dissolved in acetonitrile and treated with diethyl ether. The precipitate was allowed to settle and the supernatant discarded. The solid was dried to give the product as an off-white solid.
Workup
- customall volatiles were removed in vacuo
- washthe resulting solid was washed with ethyl acetate (twice)
- dissolutionThe remaining solid was dissolved in acetonitrile
- additiontreated with diethyl ether
- customThe solid was dried
Sources & evidence
- ORD record
- ord-ee684bf8767145cd8a18971cc4b3381d
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06057357
Reaction notes
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