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HRID 517642作成日:2026年10月27日

1,10-Phenanthroline hydrate → 7-Bromo-2-phenyl-[1,2,4]triazolo[1,5-A]pyridine

https://huagongshe.com/reaction/517642

反応式

関与物質

役割名称HCID仕込み量
反応物1,10-Phenanthroline hydrateHCID 21226—
反応物NitroxHCID 114954—
反応物2-Amino-4-bromopyridineHCID 693282—
触媒copper(I) bromideHCID 24593—
溶媒BenzonitrileHCID 7505—
生成物7-Bromo-2-phenyl-[1,2,4]triazolo[1,5-A]pyridineHCID 6777550064%

反応条件

温度130 °C

反応手順

A mixture of 2-amino-4-bromopyridine (5.00 g, 28.3 mmol), copper (I) bromide (207 mg, 1.44 mmol), 1,10-phenanthroline monohydrate (284 mg, 1.44 mmol) and benzonitrile (60 mL) was heated in a 380-mL autoclave to 130° C. and stirred for 23 h under 20 bar of O2/N2 (5:95). After the autoclave was vented and opened (100% conversion, HPLC method cf. example 1.3), the dark brown reaction suspension was then cooled to 0-5° C. and filtered. The filter cake was washed with TBME (40 mL) and dried to yield crude 7-bromo-2-phenyl-[1,2,4]triazolo[1,5-a]pyridine (5.12 g, 64%) as a green solid with 97.0% purity (HPLC area-%, HPLC method see example 1.3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115130B2
出典データセットuspto-grants-2015_08
ORD IDord-03ba9eed6cf648e3940b9cad92af2fb3
出典メモuspto-grants-2015_08