1,4-Dioxane hydrochloride → N-(5-((1R,2S)-2-(3,5-Dimethoxybenzylamino)-1-hydroxypropyl)-2-hydroxyphenyl)methanesulfonamide
Reaction equation
O1CCOCC1.[ClH:7].[CH3:8][O:9][C:10]1[CH:11]=[C:12]([CH:31]=[C:32]([O:34][CH3:35])[CH:33]=1)[CH2:13][NH:14][C@@H:15]([CH3:30])[C@@H:16]([C:18]1[CH:19]=[CH:20][C:21]([OH:29])=[C:22]([NH:24][S:25]([CH3:28])(=[O:27])=[O:26])[CH:23]=1)[OH:17]>O1CCOCC1>[ClH:7].[CH3:8][O:9][C:10]1[CH:11]=[C:12]([CH:31]=[C:32]([O:34][CH3:35])[CH:33]=1)[CH2:13][NH:14][C@@H:15]([CH3:30])[C@@H:16]([C:18]1[CH:19]=[CH:20][C:21]([OH:29])=[C:22]([NH:24][S:25]([CH3:28])(=[O:27])=[O:26])[CH:23]=1)[OH:17]Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
4N Hydrogen chloride dioxane solution (0.04 mL) was added to the dioxane solution (1 mL) of the obtained amine (4) (47 mg, 0.11 mmol), and the mixture was freeze-dried, to give hydrochloric acid salt of the amine (4) as white solid (27 mg, yield: 55%).
Workup
- customthe mixture was freeze-dried
Sources & evidence
- ORD record
- ord-74b35d516e144b2cb5352ac44c27309c
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08198330B2
Reaction notes
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