HCID 87094779, compound → HCID 66661070, compound

HRID 592275Notes

Reaction equation

HRID 592275 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5](/[CH:8]=[N:9]/[S:10]([C:12]([CH3:15])([CH3:14])[CH3:13])=[O:11])=[N:6][CH:7]=1.[CH3:16][Mg]Br>ClCCl>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C@H:8]([NH:9][S:10]([C:12]([CH3:15])([CH3:14])[CH3:13])=[O:11])[CH3:16])=[N:6][CH:7]=1

Participants

4

Procedure

To a solution of N-[(1E)-(5-fluoropyridin-2-yl)methylene]-2-methylpropane-2-sulfinamide (52.12 g, 228 mmol) in dichloromethane (1000 mL) at −78° C. was added methylmagnesium bromide (3.0 M in THF; 198 mL, 594 mmol). The mixture was allowed to warm to ambient temperature. After 30 min, the mixture was cooled down to −78° C. and was quenched with saturated aqueous ammonium chloride (100 mL). The mixture was allowed to warm to ambient temperature. The organic layer was separated and the aqueous layer was extracted with dichloromethane (3×). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% ethyl acetate) gave the title compound. MS 245 (M+1).

Workup

  1. temperaturethe mixture was cooled down to −78° C.
  2. customwas quenched with saturated aqueous ammonium chloride (100 mL)
  3. temperatureto warm to ambient temperature
  4. customThe organic layer was separated
  5. extractionthe aqueous layer was extracted with dichloromethane (3×)
  6. washThe combined organic extracts were washed with brine
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customPurification by silica gel chromatography (100% ethyl acetate)

Sources & evidence

ORD record
ord-e084d6ad1c464f73b599487886b49e49
Source dataset
uspto-grants-2016_01
Patent number
US09238647B2

Reaction notes

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