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HRID 225496作成日:2026年10月26日

Diisopropylethylamine → N-[2-[(2-Propenyloxy)-methyl]-5-nitro-phenyl}-4-(3-pyridinyl)-2-pyrimidinamine

https://huagongshe.com/reaction/225496

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-(3-Pyridyl)-3-(dimethylamino)-2-propen-1-oneHCID 567033—
反応物HCID 178459007HCID 178459007—
溶媒1-ButanolHCID 263—
溶媒Ethyl AcetateHCID 8857—
生成物N-[2-[(2-Propenyloxy)-methyl]-5-nitro-phenyl}-4-(3-pyridinyl)-2-pyrimidinamineHCID 68573992—

反応条件

温度120 °C

反応手順

A stirred mixture of {2-[(2-propenyloxy)-methyl]-5-nitro-phenyl}-guanidine (3.75 g, 15 mmol), 3-(dimethylamino)-1-(3-pyridinyl)-2-propen-1-one (2.60 g, 15 mmol) and ethyl diisopropylamine (2.6 mL, 15 mmol) in 1-butanol (50 mL) is heated at 120° C. for 20 h. The solvent is then evaporated off under reduced pressure to give a residue which is dissolved in ethyl acetate (100 mL). The resulting mixture is filtered (celite), washed with saturated aqueous sodium chloride (50 mL), dried (MgSO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by column chromatography on silica gel, eluent ethyl acetate, and recrystallised from ethyl acetate-hexane to give the title compound as a yellow crystalline solid, m.p. 213-2150C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557105B2
出典データセットuspto-grants-2009_07
ORD IDord-56d4ff03fd554ab5ade9deb49f7d226d
出典メモuspto-grants-2009_07