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HRID 986913作成日:2026年10月23日

Triethylamine hydrochloride → 7-Tert-butyl-6-chloro-3-(2-fluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/ja/reaction/986913

反応式

関与物質

役割名称HCID仕込み量
反応物Triethylamine hydrochlorideHCID 11130—
反応物4-tert-Butyl-3,6-dichloropyridazineHCID 89846—
反応物2-FluorobenzhydrazideHCID 136288—
溶媒1,4-DioxaneHCID 31275—
生成物7-Tert-butyl-6-chloro-3-(2-fluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazineHCID 1115088444%

反応手順

A mixture of 3,6-dichloro-4-(1,1-dimethylethyl)pyridazine (20 g, 0.097 mol), 2-fluorobenzhydrazide (22.6 g, 0.145 mol) and triethylamine hydrochloride (20 g, 0.0145 mol) in dioxan (1.2 l) was stirred and heated at reflux under a stream of nitrogen for 4 days. Upon cooling the volatiles were removed in vacuo and the residue was triturated with dichloromethane (200 ml), filtered and concentrated under vacuum. The residue was purified by chromatography on silica gel eluting with 0%→25% ethyl acetate/dichloromethane to give the title compound (12.95 g. 44%) as a white solid. Data for the title compound: 1H NMR (360 MHz, CDCl3) δ1.57 (9H, s), 7.26-7.35 (2H, m), 7.53-7.60 (1H, m), 7.89-7.93 (1H, m), 8.17 (1H, s); MS (ES+) m/e 305 [MH]+, 307 [MH]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06630471B1
出典データセットuspto-grants-2003_10
ORD IDord-32f104141f544d779861034672e1535e
出典メモuspto-grants-2003_10