HCID 67954034, compound → HCID 67953928, compound
Reaction equation
C(OC([N:8]([C:22]1[N:23]=[C:24]2[CH:29]=[CH:28][C:27]([Cl:30])=[CH:26][N:25]2[C:31]=1[CH3:32])[S:9]([C:12]1[CH:21]=[CH:20][C:15]([C:16]([O:18][CH3:19])=[O:17])=[CH:14][CH:13]=1)(=[O:11])=[O:10])=O)(C)(C)C>Cl.O1CCOCC1>[ClH:30].[Cl:30][C:27]1[CH:28]=[CH:29][C:24]2[N:25]([C:31]([CH3:32])=[C:22]([NH:8][S:9]([C:12]3[CH:21]=[CH:20][C:15]([C:16]([O:18][CH3:19])=[O:17])=[CH:14][CH:13]=3)(=[O:11])=[O:10])[N:23]=2)[CH:26]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Compound 15-C (0.820 g, 1.71 mmol) was dissolved in 4N HCl in dioxane (44 mL) and the reaction mixture was stirred for 24 h at room temperature. The solvent was evaporated in vacuo and the crude product was washed with ethyl ether. The resulting solid was filtered, washed with additional ethyl ether, and dried in vacuo to give compound 15-D as a white solid (0.610 g, 86%); MS m/z (M+H+) 380.
Workup
- customThe solvent was evaporated in vacuo
- washthe crude product was washed with ethyl ether
- filtrationThe resulting solid was filtered
- washwashed with additional ethyl ether
- customdried in vacuo
- customto give compound 15-D as a white solid (0.610 g, 86%)
Sources & evidence
- ORD record
- ord-7489e250853549ada7c4055f4656b305
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618150B2
Reaction notes
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