반응 #1702076

ord-35d9f80dfc074e46bceecf40ee635e71

반응 방정식

O=C([O-])O.[Na+]
sodium bicarbonate
COc1ccc2c(c1)CN(C1CC1)C(=O)CCN2
5-cyclopropyl-8-methoxy-2,3,5,6-tetrahydrobenzo[b][1,5]diazocin-4(1H)-one
O=S(=O)([O-])C(F)(F)F.O=S(=O)([O-])C(F)(F)F.[Mg+2]
magnesium trifluoromethanesulfonate
c1ccc(OCC2CO2)cc1
2-(phenoxymethyl)oxirane
COc1ccc2c(c1)CN(C1CC1)C(=O)CCN2CC(O)COc1ccccc1
desired compound
수율 65.0%
COc1ccc2c(c1)CN(C1CC1)C(=O)CCN2CC(O)COc1ccccc1
5-cyclopropyl-1-(2-hydroxy-3-phenoxypropyl)-8-methoxy-2,3,5,6-tetrahydrobenzo[b][1,5]diazocin-4(1H)-one
수율 65.0%

반응 조건

온도
75°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도After cooling to room temperature
  2. 2
    추출the mixture was extracted with dichloromethane
  3. 3
    여과The organic phases were filtered through a pad of sodium sulfate
  4. 4
    기타the filtrate evaporated

실험 절차

To a mixture of 5-cyclopropyl-8-methoxy-2,3,5,6-tetrahydrobenzo[b][1,5]diazocin-4(1H)-one (50.0 mg, 0.203 mmol) from Example 1 and magnesium trifluoromethanesulfonate (32.7 mg, 0.102 mmol) in acetonitrile (1.5 ml) was added 2-(phenoxymethyl)oxirane (30.5 mg, 0.203 mmol) and the resulting mixture was stirred at 75° C. for 100 hours. After cooling to room temperature was added sodium bicarbonate (saturated aqueous) and the mixture was extracted with dichloromethane. The organic phases were filtered through a pad of sodium sulfate and the filtrate evaporated. Preparative thin layer chromatography (EtOAc/MeOH: 95/5) of the obtained residue, gave the desired compound as a brown oil (52 mg, 65%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08765728B2uspto-grants-2014_07