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HRID 40876생성일: 2026년 10월 23일

4-Chloro-1H-pyrrolo[2,3-b]pyridine → 4-(4-bromo-3-methyl-1H-pyrazol-1-yl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/ko/reaction/40876

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11389493—
반응물HCID 178434489HCID 178434489—
생성물4-(4-bromo-3-methyl-1H-pyrazol-1-yl)-1H-pyrrolo[2,3-b]pyridineHCID 1775446587.5%

반응 조건

온도130 °C

반응 단계

A mixture of 4-chloro-1H-pyrrolo[2,3-b]pyridine (0.050 g, 0.00033 mol) and 4-bromo-3-methyl-1H-pyrazole (0.10 g, 0.00066 mol) was heated at 130° C. overnight. The reaction mixture then was subjected to column chromatography (eluting with 5% MeOH/DCM, 0.5% NH4OH, on silica gel) to give 80 mg pale yellow solid which was triturated with MeOH (1.5 mL) to yield the product as a pale yellow solid (44 mg, 44% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530485B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-0655278322ac48cd8d34c7d13d48d0cc
출처 메모uspto-grants-2013_09