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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 513생성일: 2026년 10월 23일

3-Bromopyridine → tert-butyl (3R)-3-methyl-4-pyridin-3-ylpiperazine-1-carboxylate

https://huagongshe.com/ko/reaction/513

반응식

참여 물질

역할이름HCID투입량
반응물3-BromopyridineHCID 12286—
반응물(R)-1-Boc-3-methylpiperazineHCID 2756811—
시약Sodium t-butoxideHCID 23676156—
촉매Palladium (II) acetateHCID 4144353—
촉매2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
용매TolueneHCID 1140—
생성물tert-butyl (3R)-3-methyl-4-pyridin-3-ylpiperazine-1-carboxylateHCID 89555981102.97%

반응 조건

온도100 °C

반응 단계

_Repeat of reaction EN05798-78_ Diacetoxypalladium (0.112 g, 0.50 mmol) and dicyclohexyl(2',6'-diisopropoxybiphenyl-2-yl)phosphine (0.466 g, 1.00 mmol) were dissolved in toluene (15 mL) at ambient temperature under nitrogen. The mixture was degassed and purged with nitrogen several times and heated to 50°C for 20 mins. In a separate vessel, were mixed 3-bromopyridine (0.789 g, 4.99 mmol), sodium 2-methylpropan-2-olate (0.720 g, 7.49 mmol), (R)-tert-butyl 3-methylpiperazine-1-carboxylate (1g, 4.99 mmol) and toluene (10 mL). The mixture was degassed and purged with nitrogen several times. The catalyst mixture was added to the reaction vessel and the resulting mixture was degassed and purged with nitrogen, and heated at 100 °C under nitrogen overnight. The reaction mixture was filtered through celite, washing with EtOAc/MeOH. The filtrate was concentrated and the residue purified by flash silica chromatography, elution gradient 20 to 100% EtOAc in heptane. Pure fractions were evaporated to dryness to afford (R)-tert-butyl 3-methyl-4-(pyridin-3-yl)piperazine-1-carboxylate (1.426 g, 103 %) as a pale orange gum. [Rf ~ 0.1 in 1:1 EtOAc/hept] Note: Trace Ruphos contaminating product

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-b33a6a5e9f314a52b92d41be195f749c
출처 메모750 AstraZeneca ELN dataset