Trifluoroacetic acid → 1-Methyl-2-(methylthio)-1H-pyrrole-3-sulfonamide

HRID 2259181

反応式

HRID 2259181 の反応式
CC([NH:5][S:6]([C:9]1[CH:13]=[CH:12][N:11]([CH3:14])[C:10]=1[S:15][CH3:16])(=[O:8])=[O:7])(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[CH3:14][N:11]1[CH:12]=[CH:13][C:9]([S:6]([NH2:5])(=[O:7])=[O:8])=[C:10]1[S:15][CH3:16]

参加物

4

反応物 2

HCID 6422Trifluoroacetic acidHCID 19693814N-(1,1-Dimethylethyl)-1-methyl-2-(methylthio)-1H-pyrrole-3-sulfonamide

生成物 1

HCID 196938491-Methyl-2-(methylthio)-1H-pyrrole-3-sulfonamide収率 79.6%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 4.63 g (17.66 mmol) N-(1,1-dimethylethyl)-1-methyl-2-(methylthio)-1H-pyrrole-3-sulfonamide in 50 mL of methylene chloride was added 50 mL of trifluoroacetic acid (TFA) under a nitrogen atmosphere. The orange reaction mixture was stirred at room temperature overnight ca. 16 hours. The reaction mixture was concentrated to a tan solid. Diethyl ether was added to the tan solid and was removed by evaporation to remove residual TFA. The solid was suspended in diethyl ether and filtered giving 2.9 g of the title compound as a solid, m.p. 135°-137° C. 1H NMR (Acetone-d6, 200 MHz.) δ: 6.93(d,1H), 6.45(d,1H), 6.19(bs,2H), 3.78(s,3H), 2.33(s,3H).

後処理

  1. concentrationThe reaction mixture was concentrated to a tan solid
  2. additionDiethyl ether was added to the tan solid
  3. customwas removed by evaporation
  4. customto remove residual TFA
  5. filtrationfiltered

出典と根拠

ORDレコード
ord-fa9c6b4d14d04f43b75d05948c71d030
出典データセット
uspto-grants-1995_12
特許番号
US05472933

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