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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 103생성일: 2026년 10월 23일

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(5-(benzyloxy)pyridin-2-YL)piperazine-1-carboxylate

https://huagongshe.com/ko/reaction/103

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물5-(Benzyloxy)-2-chloropyridineHCID 10013717—
시약Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
용매TolueneHCID 1140—
생성물Tert-butyl 4-(5-(benzyloxy)pyridin-2-YL)piperazine-1-carboxylateHCID 2222150368.75%

반응 조건

온도80 °C

반응 단계

BIS(DIBENZYLIDENEACETONE)PALLADIUM (0.055 g, 0.10 mmol) was added to tert- butyl piperazine-1-carboxylate (1.952 g, 10.48 mmol), 5-(benzyloxy)-2-chloropyridine (2.093 g, 9.53 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.059 g, 0.10 mmol) and sodium 2-methylpropan-2-olate (1.282 g, 13.34 mmol) in toluene (30 mL) at 20ºC under nitrogen. The resulting solution was stirred at 80 °C for 16 hours then cooled to room temperature. The reaction mixture was filtered through celite, filtrate partitioned between ethyl acetate (100 mL) and water (100 mL). The organic phase was dried (Na2SO4), filtered and evaporated to give a brown gum. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford tert-butyl 4-(5-(benzyloxy)pyridin-2-yl)piperazine-1-carboxylate (2.420 g, 68.7 %) as a yellow solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-8fcffc24262340ad8745959198669390
출처 메모750 AstraZeneca ELN dataset