Reaktion #360133

Reaktionsgleichung

4-[4-(3-Pyrrolidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-carbothioamide

bromoacetaldehyde diethylacetal

→

title compound

Ausbeute 16.0%

2-[4-(4-(3-pyrrolidin-1-ylpropoxy)phenyl)tetrahydro-2H-pyran-4-yl]-1,3-thiazole

Ausbeute 16.0%

Lösungsmittel

ethanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturheated
2. 2
   Temperaturat reflux for 5 hours
3. 3
   EinengenThe reaction mixture was concentrated in vacuo
4. 4
   Sonstigepartitioned between 10% Na2CO3 (20 mL) and dichloromethane (2×35 mL)
5. 5
   SonstigeThe combined organics were dried
6. 6
   Filtrationfiltered
7. 7
   Einengenconcentrated in vacuo
8. 8
   SonstigeThe compound was purified
9. 9
   Wascheneluting with dichloromethane:methanol:ammonia (95:5:0.5)
10. 10
    Sonstigeto give a cream
11. 11
    SonstigeThis was triturated with 3 mL of diethyl ether

Vorschrift

4-[4-(3-Pyrrolidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-carbothioamide (150 mg, 0.43 mmol), bromoacetaldehyde diethylacetal (67 μL, 0.43 mmol), concentrated hydrochloric acid (5 drops) and ethanol were combined and heated at reflux for 5 hours. The reaction mixture was concentrated in vacuo and partitioned between 10% Na2CO3 (20 mL) and dichloromethane (2×35 mL). The combined organics were dried using Na2SO4, filtered and concentrated in vacuo. The compound was purified using column chromatography using 15 g of silica gel, eluting with dichloromethane:methanol:ammonia (95:5:0.5) to give a cream coloured solid. This was triturated with 3 mL of diethyl ether to give the title compound as a cream coloured solid (25 mg, 16%). 1H NMR (400 MHz, CD3OD) δ7.7 (s, 1H), 7.45 (s, 1H), 7.3 (d, 2H), 6.9 (d, 2H), 4.0 (t, 2H), 3.8 (m, 2H), 3.7 (m, 2H), 2.85-2.75 (m, 6H), 2.6 (m, 2H), 2.4 (m, 2H), 2.03 (m, 2H), 1.9 (m, 4H)

Quelle