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HRID 712677作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物3,5-DibromopyridineHCID 69369—
反応物Binap, (A+-)-HCID 634876—
反応物Sodium t-butoxideHCID 23676156—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物4-(5-Bromopyridin-3-yl)morpholineHCID 4673961450.8%

反応条件

温度120 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181272B2
出典データセットuspto-grants-2015_11
ORD IDord-7a234e61718c4a5fb21caffcce39713f
出典メモuspto-grants-2015_11