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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3205생성일: 2026년 10월 23일

4-Ethoxyaniline → 6-(2,6-Dichlorophenyl)-2-(4-ethoxyphenylamino)-8-ethyl-8H-pyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/ko/reaction/3205

반응식

참여 물질

역할이름HCID투입량
반응물4-EthoxyanilineHCID 9076—
반응물6-(2,6-dichlorophenyl)-8-ethyl-2-methanesulfonyl-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 10596994—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물6-(2,6-Dichlorophenyl)-2-(4-ethoxyphenylamino)-8-ethyl-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 11619422—

반응 단계

A mixture of 0.150 g (0.38 mmol) of 6-(2,6-dichlorophenyl)-8-ethyl-2-methanesulfonyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 68 and 0.500 g (3.60 mmol) of 4-ethoxyaniline was fused in a 160° C. oil bath for 10 minutes. The dark violet melt was cooled and dissolved in 1 mL of warm glacial acetic acid. This solution was diluted to 10 mL volume with water to precipitate a solid. The solid was filtered, washed well with water, and dried; wt 0.140 g. Purification was effected by filtration of an ethyl acetate solution through a layer of silica gel and washing the silica gel with ethyl acetate. The filtrate was concentrated to 2 mL volume and 2 mL of petroleum ether was added. The crystals that separated on inducement were filtered and washed with ether; wt 0.094 g; mp 192°-194° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733914
출처 데이터셋uspto-grants-1998_03
ORD IDord-e03019db057645d990f6974409cc35bc
출처 메모uspto-grants-1998_03