Sodium Hydroxide → 5-Acetyl-6-methyl-2-[[(4-cyclopropylmethoxy-3-methoxy-2-pyridinyl)methyl]thio]-1H-benzimidazole

HRID 1647162Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1647162
Cl[CH2:2][C:3]1[C:8]([O:9][CH3:10])=[C:7]([O:11][CH2:12][CH:13]2[CH2:15][CH2:14]2)[CH:6]=[CH:5][N:4]=1.[C:16]([C:19]1[C:28]([CH3:29])=[CH:27][C:22]2[N:23]=[C:24]([SH:26])[NH:25][C:21]=2[CH:20]=1)(=[O:18])[CH3:17].[OH-].[Na+]>C(O)C.C(Cl)Cl.[Cl-].[Na+].O>[C:16]([C:19]1[C:28]([CH3:29])=[CH:27][C:22]2[NH:23][C:24]([S:26][CH2:2][C:3]3[C:8]([O:9][CH3:10])=[C:7]([O:11][CH2:12][CH:13]4[CH2:15][CH2:14]4)[CH:6]=[CH:5][N:4]=3)=[N:25][C:21]=2[CH:20]=1)(=[O:18])[CH3:17]

Komponenten

7

Versuchsvorschrift

2-Chloromethyl-4-cyclopropylmethoxy-3-methoxypyridine (50 mg, 0.22 mmol) and 5-acetyl-6-methyl-2-mercaptobenzimidazole (50 mg, 0.24 mmol) were dissolved in ethanol (15 ml). The pH value of the solution was adjusted to 9 (0.2M NaOH) whereupon the solution was refluxed for 10 min. After concentration of the reaction mixture at reduced pressure the residue was taken up in methylene chloride (10 ml) and brine (2 ml). The phases were separated and the organic phase was dried over sodium sulphate, filtered and concentrated at reduced pressure. The residue was chromatographed on silica (ethyl acetate). Yield: 40 mg (46%) of the title compound.

Aufarbeitung

  1. temperaturewas refluxed for 10 min
  2. customThe phases were separated
  3. dry with materialthe organic phase was dried over sodium sulphate
  4. filtrationfiltered
  5. concentrationconcentrated at reduced pressure
  6. customThe residue was chromatographed on silica (ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-433884d7ab544c598c0ce9f168894793
Quelldatensatz
uspto-grants-1995_07
Patentnummer
US05430042

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