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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2100665생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2100665

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물Diisobutylaluminum hydrideHCID 14487—
반응물Tert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylateHCID 67030211—
생성물tert-Butyl 4-(6-formylpyridin-3-yl)piperazine-1-carboxylateHCID 58181229—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07572811B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-07288dd9e14e47ea90d15f87eb67aeb8
출처 메모uspto-grants-2009_08