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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493607생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/493607

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1,1-DichloroethaneHCID 6365—
반응물Ethyl 4-amino-1-piperidinecarboxylateHCID 100867—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물N-Boc4-amino-3-pyridine carboxaldehydeHCID 20848820—
생성물Ethyl 4-[(4-[(tert-butoxycarbonyl)amino]pyridin-3-yl methyl)amino]piperidine-1-carboxylateHCID 22293255—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534784B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-20ad1e99e539418cbebf89ac90b84247
출처 메모uspto-grants-2009_05