Reaktion #586900

Reaktionsgleichung

1-methyl-4-methylaminopiperidine

1,2-dichloropropane

1,2-dichloropropane

DIC

1,2-dichloropropane

nitrophenol

4-biphenylylacetic acid

→

title compound

Ausbeute 42.0%

2-Biphenyl-4-yl-N-methyl-N-(1-methylpiperidin-4-yl)acetamide Hydrochloride

Ausbeute 42.0%

Lösungsmittel

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Filtrationfiltered
2. 2
   Waschenthe polymer was extensively washed with DCM, DMF, and 1,2-dichloropropane
3. 3
   workup.ADDITIONTo the polymer was added 1,2-dichloropropane (5 ml)
4. 4
   workup.STIRRINGThe resulting mixture was shaken at room temperature for 21 hours
5. 5
   workup.WAITat 60° C. for one hour
6. 6
   Filtrationfiltered
7. 7
   Waschenthe polymer was carefully washed with DCM and methanol
8. 8
   EinengenThe combined filtrates were concentrated
9. 9
   Sonstigeto yield the crude product, which
10. 10
    Sonstigewas purified by column chromatography (silicagel, gradient elution with DCM/methanol)
11. 11
    workup.ADDITIONThe amine was mixed with ethanol and 1 molar aqueous hydrochloric acid
12. 12
    Einengenconcentrated
13. 13
    Sonstigethe residual hydrochloride was recrystallized from acetone

Vorschrift

To the polymeric nitrophenol (1.5 g, approx. 1 mmol) was added a filtered solution of 4-biphenylylacetic acid (1.10 g, 5.18 mmol) in a mixture of 1,2-dichloropropane (18 ml) and DMF (2 ml), followed by the addition of a solution of DIC (0.63 g, 4.99 mmol) in 1,2-dichloropropane (5 ml). The mixture was shaken at room temperature for 15 hours, filtered, and the polymer was extensively washed with DCM, DMF, and 1,2-dichloropropane. To the polymer was added 1,2-dichloropropane (5 ml) and a solution of 1-methyl-4-methylaminopiperidine (0.10 g, 0.78 mmol) in 1,2-dichloropropane (10 ml). The resulting mixture was shaken at room temperature for 21 hours and then at 60° C. for one hour, filtered, and the polymer was carefully washed with DCM and methanol. The combined filtrates were concentrated to yield the crude product, which was purified by column chromatography (silicagel, gradient elution with DCM/methanol). The amine was mixed with ethanol and 1 molar aqueous hydrochloric acid, concentrated, and the residual hydrochloride was recrystallized from acetone. 120 mg (42%) of the title compound was obtained.

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