Hydrochloric Acid → HCID 23499226, compound
Reaction equation
C(OC(=O)[NH:7][CH2:8][C:9]([CH:12]1[CH2:21][CH:20]([N:22]2[C:30](=[O:31])[C:29]3[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=3)[C:23]2=[O:32])[C:19]2[C:14](=[CH:15][CH:16]=[C:17]([N+:33]([O-:35])=[O:34])[CH:18]=2)[NH:13]1)([CH3:11])[CH3:10])(C)(C)C.Cl>O1CCCC1>[NH2:7][CH2:8][C:9]([CH:12]1[CH2:21][CH:20]([N:22]2[C:23](=[O:32])[C:24]3[C:29](=[CH:28][CH:27]=[CH:26][CH:25]=3)[C:30]2=[O:31])[C:19]2[C:14](=[CH:15][CH:16]=[C:17]([N+:33]([O-:35])=[O:34])[CH:18]=2)[NH:13]1)([CH3:11])[CH3:10]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound of Example 2 (200 mg) was dissolved in 2 ml of tetrahydrofuran, and 2 ml of 2N hydrochloric acid was added. After overnight stirring at room temperature, the reaction mixture was filtered under reduced pressure. The resulting solid was dried in a vacuum to obtain 119 mg of the title compound. Its physical properties are shown below.
Workup
- filtrationthe reaction mixture was filtered under reduced pressure
- customThe resulting solid was dried in a vacuum
Sources & evidence
- ORD record
- ord-7d6cdf4729c44d75b3417a676ad2fb5c
- Source dataset
- uspto-grants-2004_08
- Patent number
- US06777427B2
Reaction notes
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