반응 #4961

반응 방정식

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

수율 82.0%

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

수율 82.0%

용매

water

반응 조건

후처리

1. 1
   기타The flask was sealed
2. 2
   workup.ADDITIONwas added
3. 3
   기타continued at room temperature
4. 4
   workup.WAITAfter 48 hr
5. 5
   기타the entire reaction mixture
6. 6
   추출extracted with 2×100 ml of benzene
7. 7
   세척washed with 3×100 ml of water and 1×100 ml saturated sodium chloride
8. 8
   건조dried over sodium sulfate
9. 9
   여과filtered
10. 10
    농축concentrated by rotary evaporation (65° C., 30 mm Hg)
11. 11
    workup.ADDITIONThe residue was treated with oxalic acid in isopropyl alcohol

실험 절차

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.

출처