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HRID 552512作成日:2026年10月25日

4-Bromo-2-methylpyridine → 6,2'-Dimethyl-[4,4']bipyridinyl-2-carboxylic acid (2-chloro-pyridin-4-yl)-amide

https://huagongshe.com/reaction/552512

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromo-2-methylpyridineHCID 2762835—
反応物N-(2-Chloropyridin-4-yl)-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carboxamideHCID 49760409—
生成物6,2'-Dimethyl-[4,4']bipyridinyl-2-carboxylic acid (2-chloro-pyridin-4-yl)-amideHCID 86614585—

反応手順

The title compound, was prepared from 6-Methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine-2-carboxylic acid (2-chloro-pyridin-4-yl)-amide in accordance with the general method of example 131, step 2 using 4-Bromo-2-methylpyridine instead of 3-Trifluoromethyl-5-bromopyridine to yield the final compound as a white solid, MS (ISP): m/e=339.1, 341.1 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07951824B2
出典データセットuspto-grants-2011_05
ORD IDord-b34e615da9dd47bf8810bf77aa74ebb9
出典メモuspto-grants-2011_05