Реакция #2358522

ord-10c84a673d2644449a9b975aeda12730

Уравнение реакции

CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
Sodium triacetoxyborohydride
CC(=O)COc1cc(F)cc(S(C)(=O)=O)c1
1-(3-fluoro-5-methylsulfonyl-phenoxy)propan-2-one
CCCN
propylamine
CC(=O)O
acetic acid
CCCNC(C)COc1cc(F)cc(S(C)(=O)=O)c1
1-(3-fluoro-5-methylsulfonyl-phenoxy)-N-propyl-propan-2-amine

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияthe suspension was filtrated
  2. 2
    workup.ADDITIONsodium carbonate (100 ml, 10% aqueous solution) was added
  3. 3
    ЭкстракцияThe aqueous phase was extracted with dichloromethane (3×50 ml)
  4. 4
    СушкаThe combined organic phase was dried with Na2SO4
  5. 5
    Другоеevaporated
  6. 6
    ДругоеPurification on flash chromatography (ethyl acetate:methanol 1:0 to 4:1)

Методика

Sodium triacetoxyborohydride (1.16 g, 5.51 mmol) was added to a stirred mixture of 1-(3-fluoro-5-methylsulfonyl-phenoxy)propan-2-one (0.905 g, 3.67 mmol), propylamine (0.24 g, 4.04 mmol), acetic acid (0.5 g, 8.33 mmol) and molecular sieves (2 g, 4 Å, 4-8 mesh) in dry 1,2-dichloroethane (20 ml) the mixture was stirred at ambient temperature for 24 h, the suspension was filtrated and sodium carbonate (100 ml, 10% aqueous solution) was added. The aqueous phase was extracted with dichloromethane (3×50 ml). The combined organic phase was dried with Na2SO4 and evaporated. Purification on flash chromatography (ethyl acetate:methanol 1:0 to 4:1). 0.3 g, 28%. MS m/z (relative intensity, 70 eV) 289 (M+, 1), 260 (9), 152 (4), 87 (6), 86 (bp).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09120728B2uspto-grants-2015_09