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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1691680생성일: 2026년 10월 27일

Triethylamine → Methyl 3-chloro-4-({[3-({[(1r)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpiperidin-1-yl]carbonyl}amino)benzoate

https://huagongshe.com/reaction/1691680

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(1R)-1-(1-naphthyl)-N-[(4-phenylpiperidin-3-yl)methyl]ethaneamineHCID 59178736—
반응물Methyl 3-chloro-4-{[(4-nitrophenoxy)carbonyl]amino}benzoateHCID 59178754—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-chloro-4-({[3-({[(1r)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpiperidin-1-yl]carbonyl}amino)benzoateHCID 59178780—

반응 단계

To a solution of 217 mg of the crude product of (1R)-1-(1-naphthyl)-N-[(4-phenylpiperidin-3-yl)methyl]ethaneamine and 0.175 mL of triethylamine in 4.0 mL of THF was added 243 mg of methyl 3-chloro-4-{[(4-nitrophenoxy)carbonyl]amino}benzoate. After stirring at room temperature overnight, the reaction mixture was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 214 mg of methyl 3-chloro-4-({[3-({[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpiperidin-1-yl]carbonyl}amino)benzoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153658B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-d001c5ae4a5b4faeac4dbbd6c5f4e121
출처 메모uspto-grants-2012_04