Water → 934282-57-2
Reaction equation
O.[Cl:2][C:3]1[CH:4]=[C:5]([C:9]2[O:13][N:12]=[C:11]([C@H:14]([O:16][C:17]3[N:18]([CH3:28])[C:19]([C:22]4[CH:27]=[CH:26][N:25]=[CH:24][CH:23]=4)=[N:20][N:21]=3)[CH3:15])[CH:10]=2)[CH:6]=[CH:7][CH:8]=1.[S:29](=[O:33])(=[O:32])([OH:31])[OH:30]>CO>[S:29]([OH:33])([OH:32])(=[O:31])=[O:30].[Cl:2][C:3]1[CH:4]=[C:5]([C:9]2[O:13][N:12]=[C:11]([C@H:14]([O:16][C:17]3[N:18]([CH3:28])[C:19]([C:22]4[CH:23]=[CH:24][N:25]=[CH:26][CH:27]=4)=[N:20][N:21]=3)[CH3:15])[CH:10]=2)[CH:6]=[CH:7][CH:8]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
An oiled salt was manufactured by evaporating a clear solution obtained by mixing 500 μl water with 33 mg 4-(5-{(1R)-1-[5-(3-chlorophenyl)isoxazol-3-yl]ethoxy}-4-methyl-4H-1,2,4-triazol-3-yl)pyridine free base, 500 μl methanol and 7 μl 98 wt-% sulphuric acid. The title salt was manufactured by recrystallising the oiled salt in 500 μl ethanol.
Workup
- customby evaporating a clear solution
- customobtained
- customby recrystallising the oiled salt in 500 μl ethanol
Sources & evidence
- ORD record
- ord-83a06e85bf604f8b98d16bc6fcbaad09
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07476684B2
Reaction notes
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