5-Bromo-2-methyl-1H-benzo[d]imidazole → HCID 58107460, Verbindung

HRID 1515463Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1515463
Br[C:2]1[CH:3]=[CH:4][C:5]2[N:9]=[C:8]([CH3:10])[NH:7][C:6]=2[CH:11]=1.C([Li])(C)(C)C.[Cl:17][C:18]1[CH:29]=[CH:28][C:21]([C:22](N(OC)C)=[O:23])=[CH:20][C:19]=1[S:30](=[O:33])(=[O:32])[NH2:31]>O1CCCC1>[Cl:17][C:18]1[CH:29]=[CH:28][C:21]([C:22]([C:2]2[CH:3]=[CH:4][C:5]3[N:9]=[C:8]([CH3:10])[NH:7][C:6]=3[CH:11]=2)=[O:23])=[CH:20][C:19]=1[S:30]([NH2:31])(=[O:33])=[O:32]

Komponenten

5

Versuchsvorschrift

A solution of 0.303 g of 6-bromo-2-methyl-1H-benzoimidazole in tetrahydrofuran (20 mL) is cooled to −50° C. and treated with 2.7 mL of tert-butyllithium (1.5 M in pentane). After 2 h at −50° C. the reaction mixture is treated with 0.12 g of 4-chloro-N-methoxy-N-methyl-3-sulfamoyl-benzamide in tetrahydrofuran (10 mL). After 3 h the mixture is quenched with saturated aqueous ammonium chloride, taken up in ethyl acetate, and washed with saturated aqueous sodium chloride. The organics are dried (magnesium sulfate), concentrated and purified by silica gel chromatography (98:2 methylene chloride/methanol) to give 2-chloro-5-(2-methyl-3H-benzoimidazole-5-carbonyl)-benzenesulfonamide. MS (m/z): 348 (M−1); Rf 0.30 (9:1 methylene chloride/methanol).

Aufarbeitung

  1. customAfter 3 h the mixture is quenched with saturated aqueous ammonium chloride
  2. washwashed with saturated aqueous sodium chloride
  3. dry with materialThe organics are dried (magnesium sulfate)
  4. concentrationconcentrated
  5. custompurified by silica gel chromatography (98:2 methylene chloride/methanol)

Quellen und Nachweise

ORD-Eintrag
ord-5d0a58efa37341b8ae8798d299496ea9
Quelldatensatz
uspto-grants-2012_07
Patentnummer
US08222424B2

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