Methanesulfonyl chloride → (S)-3-isopropylisothiazolidine 1,1-dioxide
Reaction equation
[NH2:1][C@H:2]([CH:5]([CH3:7])[CH3:6])[CH2:3]O.[CH3:8][S:9](Cl)(=[O:11])=[O:10]>>[CH:5]([C@@H:2]1[CH2:3][CH2:8][S:9](=[O:11])(=[O:10])[NH:1]1)([CH3:7])[CH3:6]Participants
3
Procedure
Using (R)-2-amino-3-methyl-1-butanol (5.0 g) and methanesulfonyl chloride (7.7 mL) and by the reaction and treatment in the same manner as in Preparation Example 1, the title compound (3.48 g) was obtained.
Workup
- customby the reaction and treatment in the same manner
- customas in Preparation Example 1
Sources & evidence
- ORD record
- ord-c546fe0dee5b4417bbcf5106f81db01e
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08816079B2
Reaction notes
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