Hydrochloric Acid → 1-Dimethylaminosulfonyl-2-acetamido-6-hydroxybenzimidazole

HRID 1758998Notes

Reaction equation

HRID 1758998 reaction equation
[CH3:1][N:2]([CH3:23])[S:3]([N:6]1[C:10]2[CH:11]=[C:12]([O:15]C(=O)C)[CH:13]=[CH:14][C:9]=2[N:8]=[C:7]1[NH:19][C:20](=[O:22])[CH3:21])(=[O:5])=[O:4].OO.Cl>CN(C)C=O>[CH3:23][N:2]([CH3:1])[S:3]([N:6]1[C:10]2[CH:11]=[C:12]([OH:15])[CH:13]=[CH:14][C:9]=2[N:8]=[C:7]1[NH:19][C:20](=[O:22])[CH3:21])(=[O:4])=[O:5]

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 784Hydrogen PeroxideHCID 132167171-Dimethylaminosulfonyl-2-acetamido-6-acetoxybenzimidazole

Product 1

HCID 132167161-Dimethylaminosulfonyl-2-acetamido-6-hydroxybenzimidazole

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

1-Dimethylaminosulfonyl-2-acetamido-6-acetoxybenzimidazole, 170 mg. (0.50 mmole), was dissolved in 3.0 ml. of dimethylformamide and 2.0 ml. of pH 10.0 buffer was added. One-half milliter of three percent hydrogen peroxide was added to the reaction mixture. The reaction mixture was allowed to stir at room temperature for about 10 minutes. The mixture was poured into 50 ml. of 0.1 N hydrochloric acid. The acid mixture was extracted with chloroform. The extract was washed successively with water and saturated sodium chloride solution. The chloroform solution was dried and evaporated in vacuo to yield 102 mg. of 1-dimethylaminosulfonyl-2-acetamido-6-hydroxybenzimidazole, mp. 175°-176° C., after crystallization

Workup

  1. dissolution(0.50 mmole), was dissolved in 3.0 ml
  2. additionof pH 10.0 buffer was added
  3. additionThe mixture was poured into 50 ml
  4. extractionThe acid mixture was extracted with chloroform
  5. washThe extract was washed successively with water and saturated sodium chloride solution
  6. dry with materialThe chloroform solution was dried
  7. customevaporated in vacuo
  8. customto yield 102 mg
  9. customof 1-dimethylaminosulfonyl-2-acetamido-6-hydroxybenzimidazole, mp. 175°-176° C., after crystallization

Sources & evidence

ORD record
ord-7e1dd70e8348496db54a7d50e190b915
Source dataset
uspto-grants-1982_07
Patent number
US04338329

Reaction notes

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