Réaction #44794

Équation de réaction

sodium bicarbonate

methyl 4-[(hexahydro-1H-diazepin-1-yl)methyl]benzoate

1-(2-iodoethoxy)-4-(benzyl)benzene

triethylamine

→

methyl 4-[[hexahydro-4-[2-[4-(phenylmethyl)phenoxy]ethyl]-1H-1,4-diazepin-1-yl]methyl]benzoate

Rendement 27.3%

Solvants

THF

Conditions de réaction

Traitement

1. 1
   Températureheated
2. 2
   Températureat reflux for 5 hours
3. 3
   TempératureAfter cooling
4. 4
   ExtractionThe mixture was extracted with ethyl acetate
5. 5
   LavageThe organic layer was washed with brine
6. 6
   Séchagedried over sodium sulfate
7. 7
   Concentrationconcentrated under reduced pressure

Mode opératoire

A mixture of methyl 4-[(hexahydro-1H-diazepin-1-yl)methyl]benzoate (109 mg, 0.44 mmol) and 1-(2-iodoethoxy)-4-(benzyl)benzene (120 mg, 0.44 mmol) in THF (4 mL) was treated with triethylamine (112 μl, 0.80 mmol) and heated at reflux for 5 hours. After cooling, the mixture was treated with saturated sodium bicarbonate solution. The mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, and concentrated under reduced pressure. Flash chromatography gave 55 mg of methyl 4-[[hexahydro-4-[2-[4-(phenylmethyl)phenoxy]ethyl]-1H-1,4-diazepin-1-yl]methyl]benzoate; 1H NMR (300 MHz, CDCl3) δ 7.98 (d, 2H), 7.42 (d, 2H), 7.28 (dd, 2H), 7.17 (d, 2H), 7.18 (dd, 1H), 7.09 (d, 2H), 6.82 (d, 2H), 4.05 (t, 2H), 3.92 (s, 2H), 3.91 (s, 3H), 3.69 (s, 2H), 2.97 (t, 2H), 2.88 (m, 2H), 2.84 (m, 2H), 2.69 (m, 4H), 1.81 (m, 2H) ppm.

Source