Reacción #1726683

Ecuación de reacción

ethyl 5-(4-chlorophenyl)-1,3,4-oxadiazole-2-carboxylate

sodium cyanide

3-hydroxyazetidine hydrochloride

triethylamine

→

2B

Rendimiento 90.0%

(5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl)(3-hydroxyazetidin-1-yl)methanone

Rendimiento 90.0%

Disolventes

Water

methanol

methanol

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrofor preparation
2. 2
   Extracciónthe mixture was extracted with dichloromethane
3. 3
   Otroevaporated to a white solid, which
4. 4
   workup.ADDITIONwas treated with toluene (5 mL)
5. 5
   Filtraciónfiltered
6. 6
   LavadoThe product was washed with toluene (5 mL)
7. 7
   Otrodried in vacuo

Procedimiento

To a suspension of ethyl 5-(4-chlorophenyl)-1,3,4-oxadiazole-2-carboxylate—for preparation, see e.g. WO 97/05131—(0.53 g, 2.10 mmol) in dry methanol (10 mL) was added sodium cyanide (20 mg, 0.42 mmol). A solution of 3-hydroxyazetidine hydrochloride (0.38 g, 2.78 mmol) and triethylamine (0.39 mL, 2.78 mmol) in methanol (10 mL) was added at ambient temperature. The mixture was stirred for 2.5 h. Water (30 mL) was added and the mixture was extracted with dichloromethane. The organic layers were combined and evaporated to a white solid, which was treated with toluene (5 mL) and then filtered. The product was washed with toluene (5 mL) and then dried in vacuo. There was obtained 0.52 g (90%) of 2B as a solid. 1H NMR (400 MHz, CD3OD): δ 4.00 (dd, 1H), 4.46 (dd, 2H), 4.70 (m, 1H), 4.93 (dd, 1H), 7.62 (d, 2H), 8.11 (d, 2H), MS (APCI+) m/z 280 [M+H]+.

Fuente