Methanol → 5-(Benzoxazol-2-yl)-2-methyl-1-(3-(morpholin-4-yl)-n-propyl)benzimidazole

HRID 74280Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 74280
N1([CH:7]([CH3:28])[CH2:8][NH:9][C:10]2[CH:15]=[CH:14][C:13]([C:16]3[O:17][C:18]4[CH:24]=[CH:23][CH:22]=[CH:21][C:19]=4[N:20]=3)=[CH:12][C:11]=2[N+:25]([O-])=O)CCOCC1.Cl.[C:30](=[NH:34])(OC)[CH3:31].[C:35](=[O:38])([O-])O.[Na+].[CH2:40](OCC)[CH3:41].[CH3:45]O>>[O:17]1[C:18]2[CH:24]=[CH:23][CH:22]=[CH:21][C:19]=2[N:20]=[C:16]1[C:13]1[CH:14]=[CH:15][C:10]2[N:9]([CH2:8][CH2:7][CH2:28][N:34]3[CH2:45][CH2:35][O:38][CH2:31][CH2:30]3)[C:40]([CH3:41])=[N:25][C:11]=2[CH:12]=1

Komponenten

6

Versuchsvorschrift

To a solution of 2-(2-(3-(morpholin-4-yl)-n-propyl)aminoanilin-4-yl)benzoxazole (see Working Example 96-1) (300 mg, 0.851 mmol) in methanol (5 mL) was added methyl acetimidate hydrochloride (103 mg, 0.936 mmol), and this was heated to reflux for 3 hours. After the reaction was complete, saturated aqueous sodium hydrogen carbonate solution was added, and this was extracted with ethyl acetate. After the organic layer obtained was dried over anhydrous sodium sulfate, it was filtered and concentrated. To the crystals obtained was added diethyl ether, this was filtered, washed with diethyl ether, and dried to yield the title compound (195 mg, 61% yield) as light brown crystals.

Aufarbeitung

  1. temperaturethis was heated
  2. temperatureto reflux for 3 hours
  3. extractionthis was extracted with ethyl acetate
  4. customAfter the organic layer obtained
  5. dry with materialwas dried over anhydrous sodium sulfate, it
  6. filtrationwas filtered
  7. concentrationconcentrated
  8. customTo the crystals obtained
  9. filtrationthis was filtered
  10. washwashed with diethyl ether
  11. customdried

Quellen und Nachweise

ORD-Eintrag
ord-e4c8259744514d4c816fc342c2a97742
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08829035B2

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