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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 517642생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/517642

반응식

참여 물질

역할이름HCID투입량
반응물1,10-Phenanthroline hydrateHCID 21226—
반응물NitroxHCID 114954—
반응물2-Amino-4-bromopyridineHCID 693282—
촉매copper(I) bromideHCID 24593—
용매BenzonitrileHCID 7505—
생성물7-Bromo-2-phenyl-[1,2,4]triazolo[1,5-A]pyridineHCID 6777550064%

반응 조건

온도130 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115130B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-03ba9eed6cf648e3940b9cad92af2fb3
출처 메모uspto-grants-2015_08