戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 493607作成日:2026年10月25日

Acetic Acid → Ethyl 4-[(4-[(tert-butoxycarbonyl)amino]pyridin-3-yl methyl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/493607

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物1,1-DichloroethaneHCID 6365—
反応物Ethyl 4-amino-1-piperidinecarboxylateHCID 100867—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物N-Boc4-amino-3-pyridine carboxaldehydeHCID 20848820—
生成物Ethyl 4-[(4-[(tert-butoxycarbonyl)amino]pyridin-3-yl methyl)amino]piperidine-1-carboxylateHCID 22293255—

反応手順

Sodium triacetoxyborohydride (1.70 g, 8.03 mmol) and acetic acid (0.29, 4.82 mmol) were added to a solution of N-Boc-4-amino-3-pyridine carboxaldehyde (0.36 g, 1.61 mmol) and ethyl 4-aminopiperidine-1-carboxylate (0.33 g, 1.93 mmol) in dichloroethane (5 mL) at room temperature. The reaction was stirred overnight, and quenched with saturated aqueous sodium bicarbonate. This was separated, extracted with ethyl acetate and the combined organics were dried over sodium sulfate. The solution was filtered and evaporated to give the crude product. This was purified by chromatography (silica gel, 0 to 12% methanol in methylene chloride gradient elution), which gave the title compound (0.24 g). MS 379.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07534784B2
出典データセットuspto-grants-2009_05
ORD IDord-20ad1e99e539418cbebf89ac90b84247
出典メモuspto-grants-2009_05