Réaction #8586

Équation de réaction

triethylamine

2-(6-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime

trifluoroacetic anhydride

→

7-chloro-2-(4-fluorophenyl)pyrazolo[1.5-α]pyridine

Rendement 68.3%

Solvants

1,2-dimethoxyethane

1,2-dimethoxyethane

Conditions de réaction

Traitement

1. 1
   Autrethe temperature below 10° C
2. 2
   workup.ADDITIONAfter the addition
3. 3
   TempératureThe solution was then cooled to 4° C.
4. 4
   TempératureAfter warming to room temperature
5. 5
   Températurethe reaction was heated
6. 6
   Températureto reflux for 3 hours
7. 7
   ConcentrationThe reaction was concentrated
8. 8
   Autrethe resulting solid was recrystallized from ethyl acetate-hexanes

Mode opératoire

To a solution of 2-(6-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime (109.2 g, 414 mmol) in 1,2-dimethoxyethane (500 mL) at 0° C. was added trifluoroacetic anhydride (59 mL, 414 mmol), keeping the temperature below 10° C. After the addition was complete, the reaction was warmed to 15° C. The solution was then cooled to 4° C. and a solution of triethylamine (116 mL, 828 mmol) in 1,2-dimethoxyethane (60 mL) was added over 0.5 hours. After warming to room temperature, the mixture was stirred for 1.5 hours. To this was added iron(II) chloride (0.52 g, 4.1 mmol) and the reaction was heated to reflux for 3 hours. The reaction was concentrated and the resulting solid was recrystallized from ethyl acetate-hexanes to give 7-chloro-2-(4-fluorophenyl)pyrazolo[1.5-α]pyridine (69.7 g. 68%) as off-white needles. 1H NMR (CDCl3): δ 8.03 (m, 2 H), 7.54 (d, 1 H), 7.16 (m, 3 H), 6.93 (d, 1 H), 6.91 (s, 1 H); MS m/z 247 (M+1); mp 156–157° C.

Source