alpha-(Aminomethyl)-2,2-dimethyl-1,3-dioxolane-4-methanol → 3-Fluoro-6-(trifluoromethylsulfamoyl)-benzoic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamide]
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:8]([S:11](=[O:18])(=[O:17])[NH:12][C:13]([F:16])([F:15])[F:14])=[CH:9][CH:10]=1)[C:5]([OH:7])=O.[OH:19][CH:20]([CH:23]1[CH2:27][O:26][C:25]([CH3:29])([CH3:28])[O:24]1)[CH2:21][NH2:22]>>[OH:19][CH:20]([CH:23]1[CH2:27][O:26][C:25]([CH3:29])([CH3:28])[O:24]1)[CH2:21][NH:22][C:5](=[O:7])[C:4]1[C:8]([S:11](=[O:18])(=[O:17])[NH:12][C:13]([F:16])([F:15])[F:14])=[CH:9][CH:10]=[C:2]([F:1])[CH:3]=1Participants
3
Procedure
Analogously to Example 22(a), 4.31 g (15 mmol) of 3-fluoro-6-(trifluoromethylsulfamoyl)-benzoic acid is reacted with 3.22 g (20 mmol) of 2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamine and the crude product is purified by chromatography on silica gel with ethyl acetate/hexane. 4.93 g=76.3% of the theoretical yield is obtained as an amorphous solid.
Workup
- customthe crude product is purified by chromatography on silica gel with ethyl acetate/hexane
- custom4.93 g=76.3% of the theoretical yield
- customis obtained as an amorphous solid
Sources & evidence
- ORD record
- ord-b5e5e2417aa24a0895bed3bd43d79bfa
- Source dataset
- uspto-grants-1992_07
- Patent number
- US05130119
Reaction notes
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