Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3209생성일: 2026년 10월 23일
Diglyme → 6-(2,6-Dichlorophenyl)-2-((4-(2-(diethylamino)ethoxy)phenyl)amino)-8-methylpyrido(2,3-d)pyrimidin-7(8H)-one
https://huagongshe.com/ko/reaction/3209
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diglyme | HCID 8150 | — |
| 반응물 | 4-(2-(Diethylamino)ethoxy)aniline | HCID 418932 | — |
| 반응물 | 6-(2,6-Dichlorophenyl)-8-methyl-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one | HCID 10736701 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 6-(2,6-Dichlorophenyl)-2-((4-(2-(diethylamino)ethoxy)phenyl)amino)-8-methylpyrido(2,3-d)pyrimidin-7(8H)-one | HCID 5311382 | — |
반응 단계
A mixture of 0.155 g (0.40 mmol) of 6-(2,6-dichlorophenyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 37, 0.167 g (0.80 mmol) of 4-(2-diethylaminoethoxy)aniline and 1 mL of (2-methoxyethyl)ether (bp 162° C.) was heated with stirring in a 150° C. oil bath. All solid gradually dissolved over a period of 10 minutes. The solution was heated another 10 minutes and cooled to 100° C. Water was added dropwise until slight turbidity. The crystals that separated on inducement were filtered, washed with 0.5 mL of ether and 2 mL of water, and dried; wt 0.105 g. Purification was effected by chromatography eluting with chloroform, then ethyl acetate and finally 10% methanol/chloroform to obtain fraction with pure product. The eluent was evaporated to dryness. The remaining amorphous solid was dissolved in 1 mL of warm ethyl acetate. The crystals that separated on inducement were filtered and washed sparingly with ethyl acetate and ether; wt 0.042 g; mp 141°-143° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05733914 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-0ccd6005f4ca42f39fa580909f4210c7 |
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| 출처 메모 | uspto-grants-1998_03 |
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