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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30065생성일: 2026년 10월 24일

2-Naphthalenecarboxaldehyde → (3R)-1-(Naphthalen-2-ylmethyl)-3-tert-butyloxycarbonylaminopyrrolidine

https://huagongshe.com/ko/reaction/30065

반응식

참여 물질

역할이름HCID투입량
반응물2-NaphthalenecarboxaldehydeHCID 6201—
반응물(3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514397—
생성물(3R)-1-(Naphthalen-2-ylmethyl)-3-tert-butyloxycarbonylaminopyrrolidineHCID 69215056—

반응 단계

This compound was prepared via the reductive amination method described in 49.2, by reaction of (R)-3-tert-butyloxycarbonylaminopyrrolidine with 2-naphthaldehyde. The residue is purified on a column of silica (eluent: from 100/0 to 90/10 (v/v) dichloromethane/methanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423030B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-a313387baa2843c19b9ac2231bc6885f
출처 메모uspto-grants-2008_09