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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 989395생성일: 2026년 10월 26일

Morpholine → 4-(2,4-Dichloro-5-methoxyanilino)-7-methoxy-8-[2-(4-morpholinyl)ethoxy]benzo[b][1,8]naphthyridine-3-carbonitrile

https://huagongshe.com/reaction/989395

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물8-(2-Chloroethoxy)-4-(2,4-dichloro-5-methoxyanilino)-7-methoxybenzo[b][1,8]naphthyridine-3-carbonitrileHCID 10164173—
반응물HCID 178506594HCID 178506594—
생성물4-(2,4-Dichloro-5-methoxyanilino)-7-methoxy-8-[2-(4-morpholinyl)ethoxy]benzo[b][1,8]naphthyridine-3-carbonitrileHCID 1016626847%

반응 단계

A mixture of 8-(2-chloroethoxy)-4-(2,4-dichloro-5-methoxyanilino)-7-methoxybenzo[b][1,8]naphthyridine-3-carbonitrile (202 mg, 0.40 mmol) and sodium iodine (70 mg, 0.47 mmol) in 4 mL of morpholine is heated at reflux for 2 hours. The reaction mixture is concentrated in vacuo and partitioned between ethyl acetate and water. The organic layer is washed with saturated sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated in vacuo. Ethyl acetate is added to the residue and the orange solid is collected by filtration to provide 105 mg (47%) of 4-(2,4-dichloro-5-methoxyanilino)-7-methoxy-8-[2-(4-morpholinyl)ethoxy]benzo[b][1,8]naphthyridine-3-carbonitrile, mp 242-244° C. dec.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06638929B2
출처 데이터셋uspto-grants-2003_10
ORD IDord-19db153b08134732ae5f8a5c6e6714eb
출처 메모uspto-grants-2003_10