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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1870745생성일: 2026년 10월 26일

Ethanol → 6-[N-(5-Chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxylic acid

https://huagongshe.com/reaction/1870745

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물6-[N-(5-Chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxamideHCID 18693258—
생성물6-[N-(5-Chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxylic acidHCID 18693249—

반응 단계

A mixture of 6-[N-(5-Chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]-pyridazine-3-carboxamide (example 18) (10.5 g, 29.3 mol) and caustic liquor, 40% w/v (10 ml, 100 mmol) in ethanol (150 ml) was stirred at reflux for 16 hours. The solvent was evaporated at reduced pressure and the residue partitioned between 2N hydrochloric acid (70 ml) and dichloromethane (200 ml). The organic layer was dried over anhydrous magnesium sulphate, filtered and evaporated to give a brown gum (10.0 g), which was redissolved in ether (200 ml) and allowed to crystallise slowly over 12 hours to give the title compound as a pale yellow solid (4.6 g, 45%) m.p. 130-131° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06100258
출처 데이터셋uspto-grants-2000_08
ORD IDord-7f5f07a5b16f4ac599d16eddc71f9b80
출처 메모uspto-grants-2000_08