Reaktion #313296

Reaktionsgleichung

8-(1-ethyl-propyl)-3-(5-fluoro-3-methyl-benzo[b]thiophen-2-yl)-2,6-dimethyl-imidazo[1,2-b]pyridazine

KOH

N,N-dimethylethanolamine

→

title compound

Ausbeute 25.1%

2-[8-(1-Ethyl-propyl)-2,6-dimethyl-imidazo[1,2-b]pyridazin-3-yl]-3-methyl-benzo[b]thiophen-5-ol

Ausbeute 25.1%

Lösungsmittel

DMSO

ethyl acetate

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeIn an oven dried
2. 2
   Sonstigenitrogen purged pressure tube
3. 3
   SonstigeThe layers are separated
4. 4
   Extraktionthe aqueous is extracted 3×50 mL of ethyl acetate
5. 5
   Trocknendried (MgSO4)
6. 6
   Einengenconcentrated under vacuum
7. 7
   SonstigeThe crude mixture is purified by chromatography
8. 8
   workup.ADDITIONThe product containing fractions

Vorschrift

In an oven dried, nitrogen purged pressure tube, 0.040 g (0.105 mmol) of 8-(1-ethyl-propyl)-3-(5-fluoro-3-methyl-benzo[b]thiophen-2-yl)-2,6-dimethyl-imidazo[1,2-b]pyridazine, 0.012 g (0.21 mmol) of KOH, and 0.019 g (0.210 mmol) of N,N-dimethylethanolamine are combined in 1 mL of dry DMSO and heated at 90° C. After approximately 24 hours, the reaction mixture is diluted with 20 mL of ethyl acetate and 20 mL of water. The layers are separated and the aqueous is extracted 3×50 mL of ethyl acetate, dried (MgSO4), and concentrated under vacuum. The crude mixture is purified by chromatography using Hexane/Ethyl Acetate. The product containing fractions are combined to obtain 0.010 g of the title compound, 25% yield. MS, ES+=380.1 (M+1); 1H NMR (DMSO-d6)=9.518 (s, 1H); 7.760-7.730 (s, 1H); 7.129 (s, 1H); 6.980 (s, 1H); 3.150-3.050 (m, 1H); 2.421 (s, 3H); 2.336 (s, 3H); 2.103 (s, 3H); 1.850-1.760 (m, 4H); 0.789-0.753 (m, 6H) ppm.

Quelle