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HRID 1922941作成日:2026年10月25日

O-Phenylenediamine → N1-(8-((4-(2-methoxypropan-2-yl)piperidin-1-yl)methyl)-9-methyl-6-morpholino-9H-purin-2-yl)benzene-1,2-diamine

https://huagongshe.com/reaction/1922941

反応式

関与物質

役割名称HCID仕込み量
反応物O-PhenylenediamineHCID 7243—
反応物Sodium t-butoxideHCID 23676156—
反応物4-(2-chloro-8-((4-(2-methoxypropan-2-yl)piperidin-1-yl)methyl)-9-methyl-9H-purin-6-yl)morpholineHCID 59605726—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
生成物N1-(8-((4-(2-methoxypropan-2-yl)piperidin-1-yl)methyl)-9-methyl-6-morpholino-9H-purin-2-yl)benzene-1,2-diamineHCID 5960554184%

反応条件

温度95 °C

反応手順

A mixture of 4-(2-chloro-8-((4-(2-methoxypropan-2-yl)piperidin-1-yl)methyl)-9-methyl-9H-purin-6-yl)morpholine (1.21 g, 2.96 mmol), benzene-1,2-diamine (520 mg, 4.8 mmol), palladium acetate (66 mg, 0.29 mmol), bist(tri-t-butylphosphine)palladium (150 mg, 0.29 mmol) and sodium t-butoxide (620 mg, 6.4 mmol) in toluene (30 mL) was stirred at 95° C. for 18 hours. The reaction mixture was then filtered through paper and then concentrated. The crude product was then purified by flash chromatography using a Biotage KP-NH column (0-10% gradient MeOH in DCM) to give N1-(8-((4-(2-methoxypropan-2-yl)piperidin-1-yl)methyl)-9-methyl-6-morpholino-9H-purin-2-yl)benzene-1,2-diamine (1.2 g, 84%). LCMS: M+H+=481.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08173650B2
出典データセットuspto-grants-2012_05
ORD IDord-58f59f5e302341899bb2a4fb9f457f7f
出典メモuspto-grants-2012_05