Hydrochloric Acid → HCID 67056666, compound
Reaction equation
Cl.[Cl:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7]([C:12]([NH:14][C@@H:15]([C@H:22]([NH:25][C:26]([C:28]1[S:29][C:30]3[CH2:31][N:32]([CH3:37])[CH2:33][CH2:34][C:35]=3[N:36]=1)=[O:27])CO)[CH2:16][C:17]([O:19][CH2:20]C)=[O:18])=[O:13])=[CH:6]2>O1CCOCC1>[ClH:2].[Cl:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7]([C:12]([NH:14][C@@H:15]1[CH2:16][C:17](=[O:18])[O:19][CH2:20][C@H:22]1[NH:25][C:26]([C:28]1[S:29][C:30]3[CH2:31][N:32]([CH3:37])[CH2:33][CH2:34][C:35]=3[N:36]=1)=[O:27])=[O:13])=[CH:6]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 4N dioxane solution (20 ml) of hydrochloric acid was added to the compound (0.31 g) obtained in Example 176, and the mixture was heated under reflux for 4 hours. The reaction mixture was concentrated, and the resultant residue was recrystallized from diethyl ether to obtain the title compound (0.23 g).
Workup
- temperaturethe mixture was heated
- temperatureunder reflux for 4 hours
- concentrationThe reaction mixture was concentrated
- customthe resultant residue was recrystallized from diethyl ether
Sources & evidence
- ORD record
- ord-c4b31d3950164f0ba11ee0bc6d391d2e
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07342014B2
Reaction notes
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