Triethylamine → N,N-Dimethyl-4,5,6,7-tetrahydro-1H-benzimidazole-1-sulfonamide
Reaktionsgleichung
[NH:1]1[C:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:4]=2[N:3]=[CH:2]1.C(N(CC)CC)C.[CH3:17][N:18]([CH3:23])[S:19](Cl)(=[O:21])=[O:20]>C(Cl)Cl>[CH3:17][N:18]([CH3:23])[S:19]([N:1]1[C:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:4]=2[N:3]=[CH:2]1)(=[O:21])=[O:20]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To solution of 4,5,6,7-tetrahydro-1H-benzoimidazole (1.9992 g, 16.4 mmol) and triethylamine (4.60 mL, 32.8 mmol) in CH2Cl2 (20 mL) at 0° C. was added dropwise a solution of dimethyl sulfamoyl chloride (1.76 mL, 16.4 mmol) in CH2Cl2 (10 mL). The reaction was warmed to room temperature and stirred for 3.5 hours. CH2Cl2 (80 mL) was added and the organic phase was washed with distilled water (1×80 mL). The aqueous washing was extracted with CH2Cl2 (2×40 mL), and the combined organic extracts were washed with brine (1×80 mL), dried (Na2SO4), and concentrated. Purification of the crude material by column chromatography on silica gel (2:1 hexanes-EtOAc) provided 2.89 g (77%) of 4,5,6,7-tetrahydro-benzoimidazole-1-sulfonic acid dimethylamide as a white solid. 1H NMR (CDCl3) δ 1.77-1.86 (m, 4H), 2.58-2.61 (m, 2H), 2.72 (t, 2H, J=6 Hz), 2.87 (s, 6H), 7.77 (s, 11H).
Aufarbeitung
- washthe organic phase was washed with distilled water (1×80 mL)
- washThe aqueous washing
- extractionwas extracted with CH2Cl2 (2×40 mL)
- washthe combined organic extracts were washed with brine (1×80 mL)
- dry with materialdried (Na2SO4)
- concentrationconcentrated
- customPurification of the crude material by column chromatography on silica gel (2:1 hexanes-EtOAc)
Quellen und Nachweise
- ORD-Eintrag
- ord-1ac032bb9a7441fca10eca4b3d93c50c
- Quelldatensatz
- uspto-grants-2008_04
- Patentnummer
- US07354932B2
Notizen zur Reaktion
Wird geladen…