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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432생성일: 2026년 10월 23일

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/ko/reaction/432

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참여 물질

역할이름HCID투입량
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물3-Bromo-2-methylpyridineHCID 1201003—
시약Sodium t-butoxideHCID 23676156—
촉매Palladium (II) acetateHCID 4144353—
촉매2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
용매TolueneHCID 1140—
생성물Tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylateHCID 6810632792.54%

반응 조건

온도100 °C

반응 단계

Palladium acetate (65 mg, 0.29 mmol) and RuPhos (271mg, 0.58mmol) were dissolved in toluene (10 mL), degassed and purged with nitrogen and warmed to 50°C for 15 minutes. In a separate vessel, were mixed 3-bromo-2-methyl pyridine (1.00g, 5.81 mmol), BOC-piperazine (1.08g, 5.81mmol), sodium tertbutoxide and toluene (17 mL). The mixture was degassed, purged with nitrogen and warmed to 50°C. The catalyst was transferred to the reaction vessel and the mixture degassed and purged with nitrogen. The reaction was heated at 100°C overnight under nitrogen. The mixture was filtered through GF/F paper, washing with MeOH. The filtrate was concentrated to provide a dark brown gum. The gum was purified by flash silica chromatography, elution gradient 30 to 80% EtOAc in heptane. Pure fractions were evaporated to provide the desired product as a gum (1.492g, 93%). Rf (1:1 EtOAc/heptane) 0.3

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-316cf52c137541f4a2a9960bf7cb84d3
출처 메모750 AstraZeneca ELN dataset