Reaktion #1137

Reaktionsgleichung

5-bromo-3-(1-methyl-2-pyrrolidinyl)pyridine

triphenylphosphine

potassium carbonate

DME

→

5-propynyl-3-(1-methyl-2-pyrrolidinyl)pyridine

Lösungsmittel

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe vessel was evacuated
2. 2
   workup.ADDITIONpropyne gas was introduced to a pressure of 20 p.s.i
3. 3
   FiltrationAnalysis by GC at this stage indicated about 40% completion and the cooled mixture was filtered through celite
4. 4
   Einengenthe filtrate concentrated in vacuo
5. 5
   Extraktionextracted with toluene (50 mL)
6. 6
   Extraktionextracted with ethyl acetate (2×100 mL)
7. 7
   WaschenThe combined ethyl acetate extracts were washed with water (50 mL)
8. 8
   Trocknendried (MgSO4)
9. 9
   Einengenconcentrated
10. 10
    Sonstigeto afford an oil
11. 11
    SonstigeThe crude product was purified by silica gel column chromatography with ethyl acetate:hexane (1:1) as eluant

Vorschrift

A Parr hydrogenation vessel was charged with 5-bromo-3-(1-methyl-2-pyrrolidinyl)pyridine (1 g, 4.15 mmol), 10% palladium on charcoal (106 mg, 0.1 mmol), copper(I)iodide (38 mg, 0.2 mmol), triphenylphosphine (104 mg, 0.4 mmol) and potassium carbonate (1.38 g, 10 mmol), DME (10 mL) and water (10 mL). The vessel was evacuated and propyne gas was introduced to a pressure of 20 p.s.i. The mixture was agitated and heated at 90° C. for 6 days, readmitting propyne gas as necessary. Analysis by GC at this stage indicated about 40% completion and the cooled mixture was filtered through celite and the filtrate concentrated in vacuo. The mixture was then acidified with 1M HCl (50 mL) and extracted with toluene (50 mL). The aqueous layer was made basic with solid potassium carbonate and extracted with ethyl acetate (2×100 mL). The combined ethyl acetate extracts were washed with water (50 mL), dried (MgSO4) and concentrated to afford an oil. The crude product was purified by silica gel column chromatography with ethyl acetate:hexane (1:1) as eluant to afford 5-propynyl-3-(1-methyl-2-pyrrolidinyl)pyridine (250 mg, 30%). A portion (225 mg) of this material was converted to the title compound by the addition of one equivalent of fumaric acid to a methanol (10 mL) solution of the free amine at 25° C. After 30 minutes the solvent was removed in vacuo and the residue pumped under high vacuum. Trituration with diethyl ether followed by recrystallization from ethyl acetate afforded 5-[1-(1-propynyl)]-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate, 180 mg, 50%. M.p. 188°-189° C. (EtOAc); 1H NMR (DMSO-d6, 300 MHz): δ 8.49 (s, 1H), 8.47 (s, 1H), 7.77 (s, 1H), 6.60 (s, 2H), 3.34 (t, J=9 Hz, 1H), 3.25 (app. t, J=9 Hz, 1H), 2.41 (dd, J=9, 9 Hz, 1H), 2.22 (m, 1H), 2.16 (s, 3H), 2.08 (s, 3H), 1.85 (m, 2H), 1.69 (m, 1H).

Quelle