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HRID 2403569作成日:2026年10月26日

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

https://huagongshe.com/reaction/2403569

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物3-Bromo-2-methylpyridineHCID 1201003—
反応物Sodium tert-butoxideHCID 45051916—
溶媒TolueneHCID 1140—
生成物Tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylateHCID 6810632798%

反応条件

温度100 °C

反応手順

3-Bromo-2-methylpyridine (500 mg) and tert-butyl piperazine-1-carboxylate (650 mg) were dissolved in toluene (7.5 ml), and (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one_palladium (3:2) (40 mg), 1,1′-binaphthalene-2,2′-diylbis(diphenylphosphine) (18 mg), and 2-methylpropan-2-ol sodium (391 mg) were added thereto in this order under a nitrogen atmosphere, followed by warming to 100° C. and stirring overnight. The reaction mixture was subjected to liquid separation with CHCl3 and water, the organic layer was dried over Na2SO4, and then the solvent was evaporated. The obtained residue was purified by silica gel column chromatography (CHCl3 to 5% MeOH/CHCl3) to obtain tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate (790 mg) as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08802679B2
出典データセットuspto-grants-2014_08
ORD IDord-98cadd563f1c443daa2dfa7faf16755c
出典メモuspto-grants-2014_08