Реакция #1509598

ord-d6895d3771b9444fb4633b6150c7789f

Уравнение реакции

O=C([O-])O.[Na+]
NaHCO3
Cc1cc(C(=O)N(C)C)cc(Cl)n1
2-Chloro-6,N,N-trimethyl-isonicotinamide
O=S(=O)(OS(=O)(=O)C(F)(F)F)C(F)(F)F
triflic anhydride
[N-]=[N+]=[N-].[Na+]
sodium azide
Cc1cc(-c2nnnn2C)cc(Cl)n1
title compound
Выход 10.7%
Cc1cc(-c2nnnn2C)cc(Cl)n1
2-Chloro-6-methyl-4-(1-methyl-1H-tetrazol-5-yl)-pyridine
Выход 10.7%

Растворители

Условия реакции

Температура
-10°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураto warm to room temperature and after 2 h
  2. 2
    Экстракцияextracted with EtOAc
  3. 3
    ДругоеThe organic layer was separated
  4. 4
    Другоеdried
  5. 5
    Концентрированиеconcentrated in vacuum

Методика

To a solution of 2-Chloro-6,N,N-trimethyl-isonicotinamide (2.3 g) in acetonitrile (30 ml) at −15° C. was added DCM (20 ml) pre-cooled triflic anhydride (3 mL) dropwise. This was stirred for 10 min at −10° C. and then sodium azide (4.6 g) was added. This was allowed to warm to room temperature and after 2 h, the reaction was neutralised with a cold 5% NaHCO3(aq) solution and extracted with EtOAc. The organic layer was separated, dried and concentrated in vacuum. Flash chromatography (100:0 to 40:60 gradient cyclohexane:EtOAc) afforded the title compound (260 mg). Rt=1.21 min (method D).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE045323E1uspto-grants-2015_01