Cesium carbonate → 4-Methoxybenzyl 4-(N-(furan-2-ylmethyl)-N-(4-methoxybenzyl)sulfamoyl)benzoate

HRID 548029

Reaktionsgleichung

Reaktionsgleichung von HRID 548029
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][NH:7][S:8]([C:11]1[CH:19]=[CH:18][C:14]([C:15]([OH:17])=[O:16])=[CH:13][CH:12]=1)(=[O:10])=[O:9].[CH3:20][O:21][C:22]1[CH:29]=[CH:28][C:25]([CH2:26]Cl)=[CH:24][CH:23]=1.[C:30](=[O:33])([O-])[O-].[Cs+].[Cs+]>CN(C=O)C.O>[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][N:7]([CH2:15][C:14]1[CH:18]=[CH:19][C:11]([O:33][CH3:30])=[CH:12][CH:13]=1)[S:8]([C:11]1[CH:19]=[CH:18][C:14]([C:15]([O:17][CH2:26][C:25]2[CH:28]=[CH:29][C:22]([O:21][CH3:20])=[CH:23][CH:24]=2)=[O:16])=[CH:13][CH:12]=1)(=[O:10])=[O:9]

Komponenten

6

Edukt 3

HCID 10796Cesium carbonateHCID 699934-Methyloxybenzyl chlorideHCID 6815254-[(Furan-2-ylmethyl)sulfamoyl]benzoic acid

Produkt 1

HCID 602089104-Methoxybenzyl 4-(N-(furan-2-ylmethyl)-N-(4-methoxybenzyl)sulfamoyl)benzoateAusbeute 160,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

4-(N-(furan-2-ylmethyl)sulfamoyl)benzoic acid (Example 5-2b) (500 mg, 1.8 mmol), p-methoxy benzyl chloride (624 mg, 4.0 mmol), and cesium carbonate (1.3 g, 4.0 mmol) were dissolved in DMF (10 mL) and stirred at 80° C. for 1 hour. The mixture was cooled to ambient temperature, diluted with H2O (200 mL), and extracted with ethyl acetate (3×100 mL). The combined organics were dried over sodium sulfate and concentrated on the rotovap. The product was purified by silica gel chromatography (15% ethyl acetate in hexanes) to provide the 4-methoxybenzyl 4-(N-(furan-2-ylmethyl)-N-(4-methoxybenzyl)sulfamoyl)benzoate (753 mg, 80%) as a clear oil. 1H NMR (DMSO-d6, 400 MHz): δ 3.70 (s, 3H), 3.75 (s, 3H), 4.22 (s, 2H), 4.26 (s, 2H), 5.39 (s, 2H), 6.14 (d, 1H, J=3.2 Hz), 6.25 (m, 1H), 6.87 (d, 2H, J=8.8 Hz), 6.97 (d, 2H, J=8.8 Hz), 7.13 (d, 2H, J=8.4 Hz), 7.39 (m, 1H), 7.43 (d, 2H, J=8.4 Hz), 7.91 (d, 2H, J=8.4 Hz), 8.07 (d, 2H, J=8.4 Hz).

Aufarbeitung

  1. temperatureThe mixture was cooled to ambient temperature
  2. extractionextracted with ethyl acetate (3×100 mL)
  3. dry with materialThe combined organics were dried over sodium sulfate
  4. concentrationconcentrated on the rotovap
  5. customThe product was purified by silica gel chromatography (15% ethyl acetate in hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-d4096539deff4affa3dc1f22fbb3da8c
Quelldatensatz
uspto-grants-2011_05
Patentnummer
US07939671B2

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