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HRID 513作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物3-BromopyridineHCID 12286—
反応物(R)-1-Boc-3-methylpiperazineHCID 2756811—
試薬Sodium t-butoxideHCID 23676156—
触媒Palladium (II) acetateHCID 4144353—
触媒2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
溶媒TolueneHCID 1140—
生成物tert-butyl (3R)-3-methyl-4-pyridin-3-ylpiperazine-1-carboxylateHCID 89555981102.97%

反応条件

温度100 °C

反応手順

_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

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-b33a6a5e9f314a52b92d41be195f749c
出典メモ750 AstraZeneca ELN dataset