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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3207생성일: 2026년 10월 24일

3,4,5-Trimethoxyaniline → 6-(2,6-Dichlorophenyl)-8-ethyl-2-(3,4,5-trimethoxyphenylamino)-8H-pyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/ko/reaction/3207

반응식

참여 물질

역할이름HCID투입량
반응물3,4,5-TrimethoxyanilineHCID 32285—
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)-8-ethyl-2-(3,4,5-trimethoxyphenylamino)-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 11540607—

반응 조건

온도160 °C

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 (2.70 mmol) of 3,4,5-trimethoxyaniline was heated in a 160° C. oil bath for 5 minutes. The dark solution was cooled and dissolved in 2 mL of warm glacial acetic acid. This solution was diluted to 15 mL volume with water to precipitate a violet solid. The solid was filtered, washed well with water, and dried; wt 0.140 g. Purification was effected by filtration of an ethyl acetate (30 mL) solution through a layer of silica gel and washing the silica gel with ethyl acetate. The filtrate was concentrated to 3 mL volume. The crystals that separated on inducement were filtered and washed with 1 mL of ethyl acetate and 1 mL of ether; wt 0.054 g; mp 275°-278° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733914
출처 데이터셋uspto-grants-1998_03
ORD IDord-76f6a432b29140da8181c2f2c78550f6
출처 메모uspto-grants-1998_03