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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1870744생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1870744

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물6-Chloropyridazine-3-carboxamideHCID 12577557—
반응물N-Ethyl 5-chloro-2-(2-methylprop-2-en-1-yloxy)benzylamineHCID 18693239—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물6-[N-(5-Chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxamideHCID 1869325858%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06100258
출처 데이터셋uspto-grants-2000_08
ORD IDord-a8bc73af172c49169e86b91fd96c8325
출처 메모uspto-grants-2000_08