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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333142생성일: 2026년 10월 24일

5-Indolylboronic acid → 5-(3-(4-aminophenyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)pyridin-2-amine

https://huagongshe.com/ko/reaction/333142

반응식

참여 물질

역할이름HCID투입량
반응물5-Indolylboronic acidHCID 2734361—
반응물3,4,5-Trimethoxybenzeneboronic acidHCID 2734390—
반응물(6-Aminopyridin-3-yl)boronic acidHCID 22396308—
반응물5-bromo-3-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridineHCID 49759066—
반응물5-bromo-3-(1H-indol-5-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridineHCID 66779176—
생성물5-(3-(4-aminophenyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)pyridin-2-amineHCID 46234191—

반응 단계

Compound Z was prepared by a method analogous to that described in Example 1 by substituting 4-aminophenylboronic acid for 1H-indol-5-ylboronic acid in the reaction with Intermediate A and 6-aminopyridin-3-ylboronic acid for 3,4,5-trimethoxyphenylboronic acid in the reaction with Intermediate B. HPLC retention time: 0.68 minutes. MS ESI (m/z): 302.4 (M+H)+, calc. 301.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877772B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-3983d3c1868546c985d608e35072042a
출처 메모uspto-grants-2014_11