Tert-Butanesulfinamide → HCID 57907608, compound

HRID 887084Notes

Reaction equation

HRID 887084 reaction equation
[Si:1]([O:8][CH:9]([C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([Cl:18])[CH:13]=1)[CH:10]=O)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[CH3:19][C:20]([S:23]([NH2:25])=[O:24])([CH3:22])[CH3:21]>ClCCl.S([O-])([O-])(=O)=O.[Cu+2]>[Si:1]([O:8][CH:9]([C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([Cl:18])[CH:13]=1)/[CH:10]=[N:25]/[S:23]([C:20]([CH3:22])([CH3:21])[CH3:19])=[O:24])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]

Participants

5

Procedure

To a solution of 3.0 g (10.6 mmol) of {[tert-butyl (dimethyl)silyl]oxy}(3-chlorophenyl)acetaldehyde (from Step C) and 1.3 g (10.6 mmol) of (R or S)-2-methyl-2-propanesulfinamide in 50 mL anhydrous dichloromethane was added copper(II) sulfate (3.4 g, 21.2 mmol) and the resulting mixture was stirred at room temperature under nitrogen atmosphere for 16 h. Wash reaction with water and extract with dichloromethane. Dry the organics with magnesium sulfate, filter and concentrate under vacuum. The residue was purified by Horizon MPLC, with a 40M+ silica gel column, eluting with a gradient eluent system of 0-25% ethyl acetate in hexane to afford the title compound (3.26 g, 80%). %). m/z (ES) 387, 390 (M, M+2)+.

Workup

  1. washWash
  2. customreaction with water
  3. extractionextract with dichloromethane
  4. dry with materialDry the organics with magnesium sulfate
  5. filtrationfilter
  6. concentrationconcentrate under vacuum
  7. customThe residue was purified by Horizon MPLC, with a 40M+ silica gel column
  8. washeluting with a gradient eluent system of 0-25% ethyl acetate in hexane

Sources & evidence

ORD record
ord-bd4c44cb41a246ad952ccda7272c0f68
Source dataset
uspto-grants-2012_08
Patent number
US08247415B2

Reaction notes

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