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HRID 40653作成日:2026年10月24日

p-Toluenesulfonic acid → 5-(4-(4-Methoxybenzylamino)-5-nitropyridin-2-ylamino)pyrazine-2-carbonitrile

https://huagongshe.com/ja/reaction/40653

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物5-Aminopyrazine-2-carbonitrileHCID 13925294—
反応物Sodium t-butoxideHCID 23676156—
反応物N-(4-Methoxybenzyl)-2-bromo-5-nitropyridin-4-amineHCID 56926468—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物5-(4-(4-Methoxybenzylamino)-5-nitropyridin-2-ylamino)pyrazine-2-carbonitrileHCID 6701745973.5%

反応条件

温度140 °C

反応手順

A mixture of palladium (II) acetate (38 mg, 0.17 mmol) and (±)-2,2″-bis(diphenylphosphino)-1,1″-binaphthalene (318 mg, 0.51 mmol) a mixture of toluene and DMF (1:1, 10 mL) was degassed under a stream of nitrogen gas with stirring for 30 minutes. After addition of 2-amino-5-cyanopyrazine (245 mg, 2.04 mmol), sodium tert-butoxide (196 mg, 2.04 mmol) and N-(4-methoxybenzyl)-2-bromo-5-nitropyridin-4-amine (575 mg, 1.70 mmol), the mixture was degassed for a further 5 minutes and then heated at 140° C. for 30 minutes in a microwave reactor. Upon cooling, the mixture was diluted with methanol and isolated by SPE using 3×2.5 g MP-TsOH cartridges, washing with methanol and then eluting with 2 M ammonia in methanol. The basic fractions were concentrated in vacuo to give the title compound (470 mg, 1.25 mmol, 73%) which was used without further purification. LCMS (2) Rt=2.18 min; m/z (ESI−) 376 (M−H); (ESI+) 378 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530468B2
出典データセットuspto-grants-2013_09
ORD IDord-6d62885f688b441e9b69920bbe819d35
出典メモuspto-grants-2013_09