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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1858641생성일: 2026년 10월 26일

Diazomethane → tert-butyl (3RS,4RS)-4-(4-methoxycarbonylmethyl-phenyl)-3-(naphthalen-2-ylmethoxy)-piperidine-1-carboxylate

https://huagongshe.com/reaction/1858641

반응식

참여 물질

역할이름HCID투입량
반응물DiazomethaneHCID 9550—
반응물(3RS,4RS)-[4-(1-tert-butoxycarbonyl-3-naphthalen-2-ylmethoxy-piperidin-4-yl)-phenyl]-acetic acidHCID 22128103—
용매DichloromethaneHCID 6344—
생성물tert-butyl (3RS,4RS)-4-(4-methoxycarbonylmethyl-phenyl)-3-(naphthalen-2-ylmethoxy)-piperidine-1-carboxylateHCID 54460902—

반응 단계

A solution of 100 mg (0.21 mmol) of (3RS,4RS)-[4-(1-tert-butoxycarbonyl-3-naphthalen-2-ylmethoxy-piperidin-4-yl)-phenyl]-acetic acid in 5 ml of methylene chloride was treated with 1 ml of ethereal diazomethane solution at room temperature and stirred for a further 2 hours. The reaction solution was evaporated under reduced pressure and the tert-butyl (3RS,4RS)-4-(4-methoxycarbonylmethyl-phenyl)-3-(naphthalen-2-ylmethoxy)-piperidine-1-carboxylate, Rf : 0.5 (hexane:ethyl acetate=2:1), obtained in quantitative yield, was used in the following step without further purification and characterization.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06150526
출처 데이터셋uspto-grants-2000_11
ORD IDord-921dd0d4625b482d954578269ddacca7
출처 메모uspto-grants-2000_11