Methanol → 1-Benzenesulfonyl-5-methylthioindole-2-carboxylic acid methyl ester

HRID 1432257Notes

Reaction equation

HRID 1432257 reaction equation
[C:1]1([S:7]([N:10]2[C:18]3[C:13](=[CH:14][C:15]([CH3:19])=[CH:16][CH:17]=3)[CH:12]=[C:11]2[C:20]([OH:22])=[S:21])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(=O)(=O)(O)O.[CH3:28]O>>[CH3:28][O:22][C:20]([C:11]1[N:10]([S:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)(=[O:8])=[O:9])[C:18]2[C:13]([CH:12]=1)=[CH:14][C:15]([CH3:19])=[CH:16][CH:17]=2)=[S:21]

Participants

4

Reactant 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 178422521HCID 178422521, compound

Product 1

HCID 865988551-Benzenesulfonyl-5-methylthioindole-2-carboxylic acid methyl ester

Procedure

A mixture of 1-benzenesulfonyl-5-methylthioindole-2-carboxylic acid (3.5 g), sulfuric acid (10 ml) and methanol (10 ml) was heated under reflux for 12 hours. The reaction mixture was poured into ice-water and extracted with dichloromethane. The organic layer was washed with water, dried overt sodium sulfate and concentrated under reduced pressure. The resulting residue, was subjected to silica, gel column chromatography (dichloromethane) to obtain 3.4 g of the desired product as a white crystal.

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for 12 hours
  3. extractionextracted with dichloromethane
  4. washThe organic layer was washed with water
  5. dry with materialdried overt sodium sulfate
  6. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-4ae87d32033e48ac93adf0ae085a6471
Source dataset
uspto-grants-2009_11
Patent number
US07612070B2

Reaction notes

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