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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 457804생성일: 2026년 10월 25일

3-(4-Piperidinyl)-1H-indole → 5-[4-(1H-indol-3-yl)-piperidin-1-ylmethyl]-2-methoxy-benzoic acid ethyl ester

https://huagongshe.com/reaction/457804

반응식

참여 물질

역할이름HCID투입량
반응물3-(4-Piperidinyl)-1H-indoleHCID 702235—
반응물5-Bromomethyl-2-methoxybenzoic acid ethyl esterHCID 68893946—
생성물5-[4-(1H-indol-3-yl)-piperidin-1-ylmethyl]-2-methoxy-benzoic acid ethyl esterHCID 6941220870%

반응 단계

This compound was prepared following the procedure described in example 1 (part D) starting with 0.2 g (1 mmol) of 3-piperidin-4-yl-1H-indole and 0.34 g (1.3 mmol) 5-bromomethyl-2-methoxy-benzoic acid ethyl ester. After ionic exchange purification, 0.273 g (70% of yield) of 5-[4-(1H-indol-3-yl)-piperidin-1-ylmethyl]-2-methoxy-benzoic acid ethyl ester were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07189741B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-8de74b28ca4b4b99b159b02ba3bbf956
출처 메모uspto-grants-2007_03