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HRID 745作成日:2026年10月23日

Ethyl 4-piperidinecarboxylate → Ethyl 1-(4-(tert-butoxycarbonyl)phenyl)piperidine-4-carboxylate

https://huagongshe.com/ja/reaction/745

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4-piperidinecarboxylateHCID 70770—
反応物Tert-butyl 4-bromobenzoateHCID 11334366—
試薬Cesium carbonateHCID 10796—
触媒Binap, (A+-)-HCID 634876—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl 1-(4-(tert-butoxycarbonyl)phenyl)piperidine-4-carboxylateHCID 190638650%

反応条件

温度110 °C

反応手順

1\. To a microwave tube was added tert-butyl 4-bromobenzoate (1.328 g, 5.16 mmol), ethyl piperidine-4-carboxylate (1.000 g, 5.16 mmol), Cs2CO3 (5.05 g, 15.49 mmol), Pd2dba3 (0.473 g, 0.52 mmol), and BINAP (0.643 g, 1.03 mmol). The mixture was dissolved in [Solvents] and sealed. The tube was de-gassed and inflated with N2. 2\. The reaction was heated at 110°C in oil-bath overnight. LCMS showed reaction complete. The reaction mixture was filter through celite pad and the solution was loaded to column for a ISCO purification (30% EtOAc in Hex). The purification is difficult with multiple by-products. Several ISCO purification was carried out and fractions were combined with other batches. Yield was poor.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-1beac9199051463f81c658e8f7cb9a0d
出典メモ750 AstraZeneca ELN dataset