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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 712677생성일: 2026년 10월 23일

Morpholine → 4-(5-Bromopyridin-3-yl)morpholine

https://huagongshe.com/ko/reaction/712677

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물3,5-DibromopyridineHCID 69369—
반응물Binap, (A+-)-HCID 634876—
반응물Sodium t-butoxideHCID 23676156—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물4-(5-Bromopyridin-3-yl)morpholineHCID 4673961450.8%

반응 조건

온도120 °C

반응 단계

In a sealable tube, to a mixture of 3,5-dibromo-pyridine (3.3 g, 13.8 mmol) and NaOtBu (0.051 g, 23 mmol) in toluene (70 mL), is added morpholine (1.0 g, 11.5 mmol). The mixture is bubbled with Argon for 5 min, and then BINAP (428.9 mg, 0.69 mmol) and Pd2(dba)3 (210.2 mg, 0.23 mmol) are added. The reaction mixture is bubbled with Argon for another 5 min. Then the cap is sealed and the reaction mixture is heated at 120° C. overnight and then is cooled to room temperature. The reaction mixture is filtered through diatomaceous earth and washed with DCM. The filtrate is partitioned between water and DCM. The aqueous phase is further extracted with DCM (2×). The combined DCM phases are concentrated. The crude is purified by flash chromatography on a silica gel column (EtOAc/heptane 0 to 50% gradient, then 50%) to provide 1.42 g of 4-(5-bromo-3-pyridyl)morpholine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181272B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-7a234e61718c4a5fb21caffcce39713f
출처 메모uspto-grants-2015_11