Реакция #170209

Уравнение реакции

tert-Butyl acrylate

diisopropylethylamine

P(o-tolyl)3

5-bromo-1H-pyrrolo[2,3-b]pyridine

→

title compound

(E)-tert-Butyl 3-(1H-pyrrolo[2,3-b]pyridin-5-yl)acrylate t-butyl acrylate

Растворители

propionitrile

dimethylformamide

Условия реакции

Обработка

1. 1
   ДругоеThe resulting mixture was purged with argon
2. 2
   ДругоеThe mixture was then purged with argon a second time
3. 3
   Температураrefluxed overnight
4. 4
   ФильтрацияThe reaction mixture was filtered on Celite®
5. 5
   КонцентрированиеThe filtrate was concentrated to dryness
6. 6
   ПромывкаThe organic layers were washed with a saturated solution of sodium chloride (3×50 mL)
7. 7
   Сушкаdried over sodium sulfate
8. 8
   Фильтрацияfiltered
9. 9
   Концентрированиеconcentrated to dryness
10. 10
    ДругоеThe crude was purified by flash chromatography on silica gel

Методика

tert-Butyl acrylate (5.9 mL, 40.6 mmol), diisopropylethylamine (3.5 mL, 20.3 mmol) and P(o-tolyl)3 (618 mg, 2.0 mmol) were successively added to a suspension of 5-bromo-1H-pyrrolo[2,3-b]pyridine (2.0 g, 10.15 mmol) in propionitrile (40 mL) and dimethylformamide (10 mL). The resulting mixture was purged with argon prior to the addition of palladium acetate (227 mg, 1.0 mmol). The mixture was then purged with argon a second time and refluxed overnight. The reaction mixture was filtered on Celite®. The filtrate was concentrated to dryness and the residue was solubilized in ethyl acetate (3×100 mL). The organic layers were washed with a saturated solution of sodium chloride (3×50 mL), dried over sodium sulfate, filtered and concentrated to dryness. The crude was purified by flash chromatography on silica gel using dichloromethane/ethyl acetate (1:0 to 7:3) as eluent. The title compound was obtained as a yellow solid (465 mg, 28%)

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