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HRID 1945961作成日:2026年10月27日

2-cyclopropyl-1H-1,3-benzodiazole → 2-(4-((2-(2-cyclopropyl-1H-benzo[d]imidazol-1-yl)-9-methyl-6-morpholino-9H-purin-8-yl)methyl)piperazin-1-yl)-2-methylpropanamide

https://huagongshe.com/reaction/1945961

反応式

関与物質

役割名称HCID仕込み量
反応物2-cyclopropyl-1H-1,3-benzodiazoleHCID 1084419—
反応物2-(4-((2-Chloro-9-methyl-6-morpholino-9H-purin-8-yl)methyl)piperazin-1-yl)-2-methylpropanamideHCID 58439189—
生成物2-(4-((2-(2-cyclopropyl-1H-benzo[d]imidazol-1-yl)-9-methyl-6-morpholino-9H-purin-8-yl)methyl)piperazin-1-yl)-2-methylpropanamideHCID 59605487—

反応手順

2-(4-((2-Chloro-9-methyl-6-morpholino-9H-purin-8-yl)methyl)piperazin-1-yl)-2-methylpropanamide (75 mg) was reacted with 2-cyclopropylbenzimidazole via General Procedure I for Buchwald coupling to give 38.7 mg 438 following reverse phase purification. MS (Q1) 559.1 (M)+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08394796B2
出典データセットuspto-grants-2013_03
ORD IDord-b3f2e2db968c40d28f29f2adb73232be
出典メモuspto-grants-2013_03