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HRID 1968424作成日:2026年10月24日

[1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-(2-methyl-5-nitro-phenyl)-amine → N3-[1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-4-methyl-benzene-1,3-diamine

https://huagongshe.com/ja/reaction/1968424

反応式

関与物質

役割名称HCID仕込み量
反応物[1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-(2-methyl-5-nitro-phenyl)-amineHCID 15949047—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物N3-[1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-4-methyl-benzene-1,3-diamineHCID 15948950—

反応手順

[1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-(2-methyl-5-nitrophenyl)-amine (135 mg, 0.37 mmol) is dissolved in ethanol (30 mL). After hydrogenation catalyzed by palladium (10 wt % on activated carbon, wet, Degussa type, 22 mg) under 1 atm H2 balloon overnight, the reaction mixture is filtered through a pad of celite and washed with ethanol. The combined filtrate and washings are concentrated to afford the title compound, which is used for next reaction without any further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08426404B2
出典データセットuspto-grants-2013_04
ORD IDord-df738a17d522404a9b50ca0761e77f2b
出典メモuspto-grants-2013_04