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HRID 1270309作成日:2026年10月25日

Potassium Carbonate → N-[2-(4-Bromophenyl)-5,7-dimethylimidazo[5,1-f][1,2,4]triazin-4-yl]-N-(3,4,5-tri-methoxyphenyl)amine

https://huagongshe.com/reaction/1270309

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物3,4,5-TrimethoxyanilineHCID 32285—
反応物2-(4-Bromophenyl)-5,7-dimethyl-4-(1H-1,2,4-triazol-1-yl)imidazo[5,1-f][1,2,4]triazineHCID 22329622—
溶媒DimethylformamideHCID 6228—
生成物N-[2-(4-Bromophenyl)-5,7-dimethylimidazo[5,1-f][1,2,4]triazin-4-yl]-N-(3,4,5-tri-methoxyphenyl)amineHCID 22329659—

反応条件

温度90 °C

反応手順

A solution of 4.0 g (10.80 mmol) of 2-(4-bromophenyl)-5,7-dimethyl-4-(1H-1,2,4-triazol-1-yl)imidazo[5,1-f][1,2,4]triazine from example 13A in DMF is treated with 2.97 g (16.21 mmol) of 3,4,5-trimethoxyaniline and 2.24 g (16.21 mmol) of potassium carbonate. The reaction mixture is stirred overnight at 90° C. After cooling, the solvent is removed on a rotary evaporator, the residue is treated twice more with toluene and the toluene is stripped off again. The crude product is extracted by stirring with a little methanol and filtered off with suction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07202243B2
出典データセットuspto-grants-2007_04
ORD IDord-5ddc2ae9ee904629825075824a6affe8
出典メモuspto-grants-2007_04