Реакция #8871

Уравнение реакции

1-(tert-butoxycarbonyl)-4-(2-hydroxyeth-1-yl)-4-(3-benzyl-(1H)-pyrazol-5-yl)piperidine

1-(tert-Butoxycarbonyl)-4-(2-hydroxyeth-1-yl)-4-(3-benzyl-(1H)-pyrazol-5-yl)piperidine

triphenylphosphine

DEAD

→

title compound

Выход 85.0%

1-(tert-Butoxycarbonyl)-2′-benzyl-5′,6′-dihydrospiro[piperidine-4,4′-[4H]pyrrolo[1,2-b]pyrazole]

Выход 85.0%

Растворители

THF

Условия реакции

Обработка

1. 1
   КонцентрированиеThe mixture was concentrated
2. 2
   Другоеpurified by flash chromatography
3. 3
   Промывкаeluting with 80% ethyl acetate in hexanes

Методика

To a solution of 1-(tert-butoxycarbonyl)-4-(2-hydroxyeth-1-yl)-4-(3-benzyl-(1H)-pyrazol-5-yl)piperidine (125 mg, 0.32 mmol) from Step I in THF (4 mL) at 0° C. was added triphenylphosphine (85 mg, 0.32 mmol) and DEAD (0.051 mL, 0.32 mmol). The reaction was stirred for 20 min and was then allowed to warm to room temperature for 2 h. The mixture was concentrated and purified by flash chromatography eluting with 80% ethyl acetate in hexanes, then 5% methanol in methylene chloride to afford the title compound (100 mg).

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