p-Toluenesulfonic acid monohydrate → 1-(4-Methanesulfonyl-phenyl)-2-thiophen-3-yl-4-trifluoromethyl-1H-imidazole

HRID 1352994ノート

反応式

HRID 1352994 の反応式
O[C:2]1([C:22]([F:25])([F:24])[F:23])[CH2:6][N:5]([C:7]2[CH:12]=[CH:11][C:10]([S:13]([CH3:16])(=[O:15])=[O:14])=[CH:9][CH:8]=2)[C:4]([C:17]2[CH:21]=[CH:20][S:19][CH:18]=2)=[N:3]1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[CH3:16][S:13]([C:10]1[CH:9]=[CH:8][C:7]([N:5]2[CH:6]=[C:2]([C:22]([F:24])([F:25])[F:23])[N:3]=[C:4]2[C:17]2[CH:21]=[CH:20][S:19][CH:18]=2)=[CH:12][CH:11]=1)(=[O:15])=[O:14]

参加物

4

反応物 2

HCID 521998p-Toluenesulfonic acid monohydrate2 回HCID 22998113HCID 22998113、化合物

生成物 1

HCID 106192741-(4-Methanesulfonyl-phenyl)-2-thiophen-3-yl-4-trifluoromethyl-1H-imidazole収率 64%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A mixture of the 4,5-dihydro-imidazole of step 2 (1.5 g, 3.8 mmol) and p-toluenesulfonic acid monohydrate (0.30 g, 1.5 mmol) in toluene (250 ml) was heated to reflux for 40 hours. An additional p-toluenesulfonic acid monohydrate (0.15.g, 0.78 mmol) was added. The reaction mixture was heated to reflux for 18 hours. The reaction mixture was cooled and the solvent removed under reduced pressure. The crude mixture (3.5 g) was purified by chromatography on silica gel using ethyl acetate/toluene (55/45) to give pure 3-[1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-1H-imidazol-2-yl]thiophene (0.90 g, 64%) as a white solid: mp 194–197° C. Anal. Calc'd. for C15H11N2S2O2F3: C, 48.38, H, 2.98, N, 7.52, S, 17.22. Found: C, 48.74, H, 2.98, N, 7.56, S. 17.45

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 40 hours
  3. temperatureThe reaction mixture was heated
  4. temperatureto reflux for 18 hours
  5. temperatureThe reaction mixture was cooled
  6. customthe solvent removed under reduced pressure
  7. customThe crude mixture (3.5 g) was purified by chromatography on silica gel

出典と根拠

ORDレコード
ord-8a05e182befb4ef79e5e015003dd7a00
出典データセット
uspto-grants-2007_05
特許番号
US07220770B2

反応ノート

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