Bromine → Methyl 5-bromo-4-methyl-3-(4-sulfamoylphenyl)thiophene-2-carboxylate

HRID 1518688ノート

反応式

HRID 1518688 の反応式
[CH3:1][C:2]1[C:3]([C:11]2[CH:16]=[CH:15][C:14]([S:17](=[O:20])(=[O:19])[NH2:18])=[CH:13][CH:12]=2)=[C:4]([C:7]([O:9][CH3:10])=[O:8])[S:5][CH:6]=1.[Br:21]Br>C(Cl)Cl>[Br:21][C:6]1[S:5][C:4]([C:7]([O:9][CH3:10])=[O:8])=[C:3]([C:11]2[CH:16]=[CH:15][C:14]([S:17](=[O:20])(=[O:19])[NH2:18])=[CH:13][CH:12]=2)[C:2]=1[CH3:1]

参加物

4

反応条件

温度
25 °C

実験手順

To a stirred suspension of methyl 4-methyl-3-(4-sulfamoylphenyl)thiophene-2-carboxylate (compound 7b, 8.80 g, 27.0 mmol) in DCM (150 ml), bromine (5.19 g, 1.67 ml, 32.0 mmol) was added at 0° C. in a drop wise manner. The reaction mixture was stirred at 25° C. for 2 hr and the progress of the reaction was monitored by TLC. The reaction mixture was then concentrated completely and again dissolved in DCM (250 ml). The organic layer so obtained was washed with water (2×50 ml), brine (1×50 ml) and dried over sodium sulfate and concentrated under reduced pressure to obtain crude product as semi-solid (10.2 g), which was then purified by column chromatography over silica gel (100-200 mesh) using 50% ethyl acetate in hexanes as an eluent to obtain the title compound (20% ethyl ester as trans esterified product was observed) (9.0 g, 82.34%).

後処理

  1. additionwas added at 0° C. in a drop wise manner
  2. concentrationThe reaction mixture was then concentrated completely
  3. dissolutionagain dissolved in DCM (250 ml)
  4. customThe organic layer so obtained
  5. washwas washed with water (2×50 ml), brine (1×50 ml)
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customto obtain crude product as semi-solid (10.2 g), which
  9. customwas then purified by column chromatography over silica gel (100-200 mesh)

出典と根拠

ORDレコード
ord-b1076ce20fe8486c9c2fdb32513e585f
出典データセット
uspto-grants-2015_07
特許番号
US09072731B2

反応ノート

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