Reaktion #4961

Reaktionsgleichung

azetidine

azetidine

7-chloro-2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepine-5(4H)-thione

potassium carbonate

azetidine

dimethyl sulfoxide

→

yellow crystals

Ausbeute 82.0%

2-(1-Azetidinyl]ethyl-7-chloro-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepine-5(4H)-thione oxalate

Ausbeute 82.0%

Lösungsmittel

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe flask was sealed
2. 2
   workup.ADDITIONwas added
3. 3
   Sonstigecontinued at room temperature
4. 4
   workup.WAITAfter 48 hr
5. 5
   Sonstigethe entire reaction mixture
6. 6
   Extraktionextracted with 2×100 ml of benzene
7. 7
   Waschenwashed with 3×100 ml of water and 1×100 ml saturated sodium chloride
8. 8
   Trocknendried over sodium sulfate
9. 9
   Filtrationfiltered
10. 10
    Einengenconcentrated by rotary evaporation (65° C., 30 mm Hg)
11. 11
    workup.ADDITIONThe residue was treated with oxalic acid in isopropyl alcohol

Vorschrift

To a solution of 4.75 g (0.0164 mole) of 7-chloro-2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepine-5(4H)-thione in 40 ml of dimethyl sulfoxide was added 8.0 g of crushed potassium carbonate and 1.4 g (0.0246 mole) of azetidine. The flask was sealed and stirred at room temperature for 24 hr after which an additional 0.6 g (0.011 mole) of azetidine was added. After 24 hr, another 0.5 (0.009 mole) of azetidine was added and stirring continued at room temperature. After 48 hr, the entire reaction mixture was diluted with 200 ml of water and extracted with 2×100 ml of benzene. The organic extracts were combined, washed with 3×100 ml of water and 1×100 ml saturated sodium chloride, dried over sodium sulfate, filtered, and concentrated by rotary evaporation (65° C., 30 mm Hg). The residue was treated with oxalic acid in isopropyl alcohol to give 5.4 g (82%) of yellow crystals, m.p. 146°-150° C.

Quelle