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HRID 40876作成日:2026年10月24日

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/ja/reaction/40876

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11389493—
反応物HCID 178434489HCID 178434489—
生成物4-(4-bromo-3-methyl-1H-pyrazol-1-yl)-1H-pyrrolo[2,3-b]pyridineHCID 1775446587.5%

反応条件

温度130 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530485B2
出典データセットuspto-grants-2013_09
ORD IDord-0655278322ac48cd8d34c7d13d48d0cc
出典メモuspto-grants-2013_09