Diethyl disulfide → HCID 12056497, compound

HRID 990618Notes

Reaction equation

HRID 990618 reaction equation
Br[C:2]([F:19])([F:18])[S:3]([C:6]1[N:10]=[CH:9][N:8]([C:11](=[O:17])[N:12]([CH2:15][CH3:16])[CH2:13][CH3:14])[N:7]=1)(=[O:5])=[O:4].[CH2:20]([S:22]SCC)[CH3:21].P([O-])([O-])(O)=O.[Na+].[Na+].S(S([O-])=O)([O-])=O.[Na+].[Na+]>CN(C)C=O.O>[CH2:13]([N:12]([CH2:15][CH3:16])[C:11]([N:8]1[CH:9]=[N:10][C:6]([S:3]([C:2]([F:19])([F:18])[S:22][CH2:20][CH3:21])(=[O:5])=[O:4])=[N:7]1)=[O:17])[CH3:14]

Participants

7

Reactant 4

HCID 8077Diethyl disulfideHCID 24203Sodium Phosphate, DibasicHCID 24489Sodium DithioniteHCID 12056494HCID 12056494, compound

Product 1

HCID 12056497HCID 12056497, compoundYield 57%

Reagents, catalysts & solvents 2

HCID 962WaterSolvent2×HCID 6228DimethylformamideSolvent

Procedure

To a stirred solution of 10 g (0.028 mol) 3-(bromodifluoromethylsulfonyl)-1-(N,N-diethylcarbamoyl)-1,2,4-triazole (as prepared in Example 1) and 6.81 ml (0.055 mol) diethyl disulfide in a mixture of 30 ml N,N-dimethylformamide and 20 ml water at 0° C. was added 5.9 g (0.042 mol) sodium hydrogen phosphate and 7.23 g (0.042 mol) sodium dithionite. After 2 h, the reaction mixture was diluted with 100 ml water and extracted with ethyl acetate (3×100 ml). The combined resulting organic layers were washed with saturated sodium chloride solution, dried over MgSO4 and evaporated. Preparative LC purification of the residue with 40% ethyl acetate-hexane gave 5.45 g (57% yield) of the desired 1-(N,N-diethylcarbamoyl)-3-[difluoro(ethylthio)methylsulfonyl]-1,2,4-triazole as a colorless oil having n D 25 = 1.5063 .

Workup

  1. extractionextracted with ethyl acetate (3×100 ml)
  2. customThe combined resulting organic layers
  3. washwere washed with saturated sodium chloride solution
  4. dry with materialdried over MgSO4
  5. customevaporated
  6. customPreparative LC purification of the residue with 40% ethyl acetate-hexane

Sources & evidence

ORD record
ord-a7b3aa5ce184474cbc1429c8204dc36b
Source dataset
uspto-grants-2002_10
Patent number
US06461997B1

Reaction notes

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