Methanesulfonyl chloride → (S)-3-isopropylisothiazolidine 1,1-dioxide

HRID 2411129Notes

Reaction equation

HRID 2411129 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

  1. customby the reaction and treatment in the same manner
  2. 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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