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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271894생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/271894

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 번호US07452903B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-473713cae8484bffb0da7f0df6d994ea
출처 메모uspto-grants-2008_11