Dimethyl Sulfoxide → HCID 14086958, compound

HRID 2173327Notes

Reaction equation

HRID 2173327 reaction equation
[CH3:1][S:2]([CH3:4])=O.O(S(C(F)(F)F)(=O)=O)S(C(F)(F)F)(=O)=O.[Br:20][C:21]1[N:22]=[CH:23][C:24]([NH2:27])=[N:25][CH:26]=1>C(Cl)Cl>[Br:20][C:21]1[CH:26]=[N:25][C:24]([N:27]=[S:2]([CH3:4])[CH3:1])=[CH:23][N:22]=1

Participants

5

Conditions

Temperature
-70 °C

Procedure

To a solution of DMSO (11 g, 138 mmol) in 100 mL of DCM was added Tf2O (42 g, 149 mmol) at −70° C. The resulting mixture was stirred at −70° C. for 15 minutes then a solution of 5-bromopyrazin-2-amine (20 g, 115 mmol, in 100 mL of DCM and 50 mL of DMSO) was added dropwise. The mixture was stirred at −60° C. for 3 hours and diluted with 500 mL of DCM and washed with water. The water layer was basified to pH=11 with aq. Na2CO3 and extracted with DCM twice. The combined DCM layer was washed with brine, dried over Na2SO4 and evaporated to afford 2-bromo-5-[(dimethyl-λ4-sulfanylidene)amino]pyrazine. 1H-NMR (CDCl3, 400 MHz) δ 7.89 (s, 1H), 7.78 (s, 1H), 2.72 (s, 6H).

Workup

  1. stirringThe mixture was stirred at −60° C. for 3 hours
  2. washwashed with water
  3. extractionextracted with DCM twice
  4. washThe combined DCM layer was washed with brine
  5. dry with materialdried over Na2SO4
  6. customevaporated

Sources & evidence

ORD record
ord-bb6ec17b7c6f4e6eba2101612a2e29cb
Source dataset
uspto-grants-2015_06
Patent number
US09056859B2

Reaction notes

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