Hydrochloric Acid → Da-6886

HRID 1506936Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1506936
[NH2:1][C:2]1[C:10]([Cl:11])=[CH:9][C:5](C(N)=O)=[C:4]([O:12][CH3:13])[C:3]=1CC1CCNCC1.Cl.CS(O[CH2:27][CH2:28][CH2:29][N:30]1[CH:34]=[CH:33][N:32]=[N:31]1)(=O)=O.C([N:37]([CH2:40][CH3:41])[CH2:38][CH3:39])C.[C:42](=O)([O-])[O-].[K+].[K+].[I-].[K+].[CH3:50][N:51](C)[CH:52]=[O:53]>>[N:30]1([CH2:29][CH2:28][CH2:27][N:37]2[CH2:38][CH2:39][CH:42]([CH2:50][NH:51][C:52](=[O:53])[C:5]3[CH:9]=[C:10]([Cl:11])[C:2]([NH2:1])=[CH:3][C:4]=3[O:12][CH3:13])[CH2:41][CH2:40]2)[CH:34]=[CH:33][N:32]=[N:31]1

Komponenten

8

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

4-amino-5-chloro-2-methoxy-(piperidin-4-ylmethyl)benzamide (compound of formula 2) hydrochloride (400 mg, 1.2 mmol) was dissolved in dimethylformamide (10 mL), and 3-(1,2,3-triazol-1-yl)propyl methanesulfonate (compound of formula 3) (344 mg, 1.68 mmol), triethylamine (0.5 mL, 3.591 mmol), potassium carbonate (232 mg, 1.68 mmol), and potassium iodide (40 mg, 0.24 mmol) were added thereto, followed by stirring at 120° C. for 4 hours. After the reaction was completed, the reactants were cooled to room temperature, extracted with ethyl acetate and water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting residue was purified by column chromatography to afford the title compound (185 mg, 38%).

Aufarbeitung

  1. temperaturethe reactants were cooled to room temperature
  2. extractionextracted with ethyl acetate and water
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe resulting residue was purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-a4574c81ae6b45b2bf0de9ec33dfeb9c
Quelldatensatz
uspto-grants-2015_12
Patentnummer
US09221790B2

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