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HRID 2100665作成日:2026年10月27日

Hydrochloric Acid → tert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2100665

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TetrahydrofuranHCID 8028—
反応物Diisobutylaluminum hydrideHCID 14487—
反応物Tert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylateHCID 67030211—
生成物tert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylateHCID 58181229—

反応手順

To a solution of tert-butyl 4-(6-cyano-pyridin-3-yl)-piperazine-1-carboxylate (2.15 mmol) in THF (20 mL) is added a solution of DIBAL-H in THF (1.0 M, 13 mmol) dropwise and the reaction mixture is stirred at room temperature for 15 minutes. After it is cooled to 0° C., the reaction mixture is mixed with a solution of aqueous HCl (2 N, 5 mL) after which the reaction mixture is partitioned between saturated Na2CO3 solution and EtOAc. The aqueous phase is extracted with EtOAc. The combined organic extracts are washed with saturated aqueous NaCl and dried over Na2SO4. After concentration, the residue is purified by silica gel chromatography (3:7 hexanes/EtOAc) to give tert-butyl 4-(6-formyl-pyridin-3-yl)-piperazine-1-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07572811B2
出典データセットuspto-grants-2009_08
ORD IDord-07288dd9e14e47ea90d15f87eb67aeb8
出典メモuspto-grants-2009_08