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HRID 1870744作成日:2026年10月27日

Diisopropylethylamine → 6-[N-(5-Chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxamide

https://huagongshe.com/reaction/1870744

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物6-Chloropyridazine-3-carboxamideHCID 12577557—
反応物N-Ethyl 5-chloro-2-(2-methylprop-2-en-1-yloxy)benzylamineHCID 18693239—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物6-[N-(5-Chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxamideHCID 1869325858%

反応手順

A mixture of N-ethyl-5-chloro-2-(2-methylprop-2-en-1-yloxy)benzylamine (reference example 16) (13.8 g, 50 mM), 6-chloropyridazine-3-carboxamide (7.9 g, 50 mM) and di-isopropylethylamine (20.0 ml, 115 mM) in DMF (50 ml) was stirred at reflux for 16 hours. The mixture was cooled and diluted with water (200 ml) giving an oil which was allowed to settle out (1 hour). The supernatant liquor was decanted and the residual brown gum dissolved in dichloromethane (250 ml) and washed with 2N hydrochloric acid (100 ml). The product was obtained by eluting the organic layer through silica, adjusting the solvent to dichloromethane/isopropanol (19:1) and collecting relevant fractions, which were combined and evaporated to give the title compound as a gum (10.5 g, 58%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06100258
出典データセットuspto-grants-2000_08
ORD IDord-a8bc73af172c49169e86b91fd96c8325
出典メモuspto-grants-2000_08