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HRID 1677485作成日:2026年10月27日

4-(4-tert-Butoxycarbonylpiperazinyl)phenylboronic acid, pinacol ester → 4-{4-[7-(1-Methyl-cyclohexanecarbonyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1677485

反応式

関与物質

役割名称HCID仕込み量
反応物4-(4-tert-Butoxycarbonylpiperazinyl)phenylboronic acid, pinacol esterHCID 2795514—
反応物(2-bromo-5H-pyrrolo[2,3-b]pyrazin-7-yl)-(1-methyl-cyclohexyl)-methanoneHCID 44199730—
生成物4-{4-[7-(1-Methyl-cyclohexanecarbonyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl]-phenyl}-piperazine-1-carboxylic acid tert-butyl esterHCID 59540697—

反応手順

4-{4-[7-(1-Methyl-cyclohexanecarbonyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester was prepared starting from (2-bromo-5H-pyrrolo[2,3-b]pyrazin-7-yl)-(1-methyl-cyclohexyl)-methanone and 4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-piperazine-1-carboxylic acid tert-butyl ester following general procedures as described in these Examples. M+H=504.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08008298B2
出典データセットuspto-grants-2011_08
ORD IDord-4d23d3c9fd6c47abb2c36a2f09f7c5cc
出典メモuspto-grants-2011_08