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HRID 227682作成日:2026年10月25日

2,4-Dimethoxybenzylamine → 2-(2,4-dimethoxybenzylamino)carbonyl-3-(4-nitrophenyl)-1H-pyrrole

https://huagongshe.com/reaction/227682

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-DimethoxybenzylamineHCID 597250—
反応物TrimethylaluminumHCID 16682925—
反応物methyl 3-(4-nitrophenyl)-1H-pyrrole-2-carboxylateHCID 18616331—
溶媒TolueneHCID 1140—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物2-(2,4-dimethoxybenzylamino)carbonyl-3-(4-nitrophenyl)-1H-pyrroleHCID 5775687864.9%

反応条件

温度20 °C

反応手順

To 2.435 cm3 (15.84 mmol) of 2,4-dimethoxybenzylamine dissolved in 65 cm3 of toluene are added, at a temperature in the region of 20° C. under an argon atmosphere, 10.3 cm3 (20.59 mmol) of a 2M solution of trimethylaluminium in toluene, followed by addition of 1.95 g (7.92 mmol) of methyl 3-(4-nitrophenyl)-1H-pyrrole-2-carboxylate. After stirring for 1 hour at a temperature in the region of 20° C. and then for 16 hours at a temperature in the region of 60° C., the reaction mixture is diluted with 170 cm3 of ethyl acetate. The resulting solution is washed successively with three times 70 cm3 of saturated aqueous ammonium chloride solution and twice 50 cm3 of water and then dried over anhydrous magnesium sulfate, filtered and concentrated to dryness under reduced pressure (2.7 kPa) to give a yellow solid, which is then stirred in 20 cm3 of acetonitrile at a temperature in the region of 5° C. for 30 minutes. After filtering through a No. 3 sinter funnel, the solid is washed with 10 cm3 of ice-cold acetonitrile and then dried under reduced pressure (2.7 kPa) at a temperature in the region of 35° C. for 3 hours to give 1.96 g of 2-(2,4-dimethoxybenzylamino)carbonyl-3-(4-nitrophenyl)-1H-pyrrole in the form of a yellow solid; ES+: m/z=382: [M+H]+; ES−: m/z=380: [M−H]−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560571B2
出典データセットuspto-grants-2009_07
ORD IDord-e99534bacea84e6baf689b8773f7cf87
出典メモuspto-grants-2009_07