Reaction #321628

ord-0c102bb41af1487a80c8ad5409671aab

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherN-[5-(4-methylphenyl)thiophene-2-sulfonyl]pyrrole was prepared in the same manner
  2. 2
    OtherPurification by column chromatography

Procedure

N-[5-(4-methylphenyl)thiophene-2-sulfonyl]pyrrole was prepared in the same manner as described in Example 32C using 4-methyl-phenylboronic acid and N-(5-bromothiophenesulfonyl)pyrrole. Purification by column chromatography using 2% ethyl acetate/hexanes gave N-[5-(4-methylphenyl)thiophene-2-sulfonyl]pyrrole as a pale yellow solid in 77% yield.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05594021uspto-grants-1997_01