HCID 68528117, compound → HCID 68526678, compound

HRID 1445507Notes

Reaction equation

HRID 1445507 reaction equation
C([O:5][C:6](=[O:24])/[CH:7]=[CH:8]/[C:9]1[CH:13]=[CH:12][N:11]([S:14]([C:17]2[CH:22]=[CH:21][C:20]([I:23])=[CH:19][CH:18]=2)(=[O:16])=[O:15])[CH:10]=1)(C)(C)C>ClCCl.C(O)(C(F)(F)F)=O>[I:23][C:20]1[CH:19]=[CH:18][C:17]([S:14]([N:11]2[CH:12]=[CH:13][C:9](/[CH:8]=[CH:7]/[C:6]([OH:24])=[O:5])=[CH:10]2)(=[O:16])=[O:15])=[CH:22][CH:21]=1

Participants

4

Procedure

A mixture of 6.69 g (E)-3-[1-(4-Iodo-benzenesulfonyl)-1H-pyrrol-3-yl]-acrylic acid tert-butyl ester in 180 ml dichloromethane and 18.1 ml TFA is stirred at ambient temperature over the weekend. The reaction mixture is evaporated and the crude product is washed with toluene and dried in vacuo.

Workup

  1. customThe reaction mixture is evaporated
  2. washthe crude product is washed with toluene
  3. customdried in vacuo

Sources & evidence

ORD record
ord-e1e1b5ac2bc048cc868f9ecd032a6c6d
Source dataset
uspto-grants-2010_02
Patent number
US07666868B2

Reaction notes

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