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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327생성일: 2026년 10월 24일

3,5-Dibromopyridine → 3-bromo-5-[(3R)-3-methoxypyrrolidin-1-yl]pyridine

https://huagongshe.com/ko/reaction/327

반응식

참여 물질

역할이름HCID투입량
반응물3,5-DibromopyridineHCID 69369—
반응물(R)-3-MethoxypyrrolidineHCID 15086791—
시약Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물3-bromo-5-[(3R)-3-methoxypyrrolidin-1-yl]pyridineHCID 5761362551.14%

반응 조건

온도90 °C

반응 단계

A mixture of 3,5-dibromopyridine (0.644 g, 2.72 mmol), (R)-3-methoxypyrrolidine (0.25 g, 2.47 mmol), TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM (0.045 g, 0.05 mmol), sodium 2-methylpropan-2-olate (0.356 g, 3.71 mmol) and 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.077 g, 0.12 mmol) in degassed toluene (7.5 ml) was sealed into a microwave tube and stirred for 16 hours at 90 °C. The reaction was completed. After cooling, an aqueous solution of Na2CO3 was added. Extraction with DCM (twice). The organic layers were dried over MgSO4 and evaporated _in vacuo_ to give the crude product as an orange oil. PBO-04062-54-01 It was purified by chromatography (Merck cartridge SVF D26 - SI60 15-40 µm - 30 g) on silica gel eluting with EtOAc 0 to 25% in petroleum ether. Pure collected fractions were evaporated to afford (R)-3-bromo-5-(3-methoxypyrrolidin-1-yl)pyridine (0.325 g, 51.1 %) as a yellow oil. PBO-04062-54-02

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-29d169023edf45ffb5746904d99b3825
출처 메모750 AstraZeneca ELN dataset