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HRID 448123作成日:2026年10月26日

Methanol → 4-Chloro-2-[1,2,4]triazolo[4,3-a]pyrimidin-3-yl-phenylamine

https://huagongshe.com/reaction/448123

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物5-Chloro-2-nitrobenzaldehydeHCID 81123—
反応物2-HydrazinylpyrimidineHCID 346558—
反応物Iodo benzene diacetateHCID 12217721—
触媒IronHCID 23925—
溶媒EthanolHCID 702—
溶媒Ammonium ChlorideHCID 25517—
生成物4-Chloro-2-[1,2,4]triazolo[4,3-a]pyrimidin-3-yl-phenylamineHCID 43628644—

反応条件

温度60 °C

反応手順

A 5 mL scintillation vial was charged with 2-hydrazinopyrimidine (61 mg, 0.55 mmol), 2-nitro-5-chlorobenzaldehyde (112 mg, 0.60 mmol) and MeOH (500 μL) and heated to 60° C. for 30 minutes. The MeOH was then removed in vacuo and the resultant solid was washed with Et2O. The crude solid (30 mg) was then suspended in CH2Cl2 (1 mL) and iodobenzene diacetate (39 mg, 0.12 mmol) was added. The reaction was stirred at room temperature for 30 minutes after which the solvent was removed in vacuo. The resultant residue was then dissolved in a 10% solution of saturated NH4Cl(aq) in EtOH and iron (19 mg, 0.33 mmol) was then added and the reaction was stirred at 80° C. for 4 h. The solvent was then removed in vacuo and the product was purified by silica gel chromatography to afford 4-chloro-2-[1,2,4]triazolo[4,3-a]pyrimidin-3-yl-phenylamine as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481579B2
出典データセットuspto-grants-2013_07
ORD IDord-0b6bc742720c489698823c3cb82c3e17
出典メモuspto-grants-2013_07