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HRID 472531作成日:2026年10月27日

2-Methoxy-5-(trifluoromethyl)phenylboronic acid → 2-Chloro-5-(2-methoxy-5-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridine

https://huagongshe.com/reaction/472531

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methoxy-5-(trifluoromethyl)phenylboronic acidHCID 2782676—
反応物8-Bromo-2-chloro-[1,2,4]triazolo[1,5-a]pyridineHCID 67481370—
生成物2-Chloro-5-(2-methoxy-5-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridineHCID 67479123—

反応手順

2-Chloro-5-(2-methoxy-5-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridine was prepared from 8-bromo-2-chloro[1,2,4]triazolo[1,5-a]pyridine (0.5 g, 2.15 mmol) and 2-methoxy-5-trifluoromethylbenzeneboronic acid (0.71 g, 3.23 mmol) in a manner analogous to Example 2c. Product was isolated as a foam (0.7 g, 82%). 1H NMR (400 MHz, CDCl3, δ, ppm): 7.80 (d, J=8.8 Hz, 1H), 7.75-7.70 (m, 2H), 7.68-7.62 (m, 1H), 7.16 (d, J=8.8 Hz, 1H), 7.09 (d, J=6.8 Hz, 1H), 3.87 (s, 3H). MS=328 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633173B2
出典データセットuspto-grants-2014_01
ORD IDord-362330d52bd24e4da831ec50d46e63af
出典メモuspto-grants-2014_01