Reaktion #165065
ord-46d5cd948674461d9956f6455fb5cacc
Reaktionsgleichung
4-bromopyrazole
trans-1,2-cyclohexanediamine
potassium carbonate
N-(3-iodo-pyridin-2-yl)-2,2-dimethyl-propionamide
→
title compound
Ausbeute 53.4%
N-(3-(4-Bromo-pyrazol-1-yl)-pyridin-2-yl)-2,2-dimethyl-propionamide
Ausbeute 53.4%
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Temperatur
110°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1EinengenThe reaction mixture was concentrated under a reduced pressure
- 2SonstigeThe residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=2:1)
Vorschrift
To a mixture of N-(3-iodo-pyridin-2-yl)-2,2-dimethyl-propionamide (380 mg, 1.2 mmol) described in Manufacturing Example 39-1-2 and toluene (10 mL) were added 4-bromopyrazole (160 mg, 1.1 mmol), copper (I) iodide (11 mg, 0.056 mmol), trans-1,2-cyclohexanediamine (26 mg, 0.22 mmol) and potassium carbonate (340 mg, 2.5 mmol) at room temperature, which was stirred overnight at 110° C. The reaction mixture was concentrated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=2:1) to obtain the title compound (190 mg, 52%).