Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3188생성일: 2026년 10월 23일
N-(3-Aminopropyl)morpholine → 6-(2,6-dichlorophenyl)-8-methyl-2-{[3-(morpholin-4-yl)propyl]amino}-7H,8H-pyrido[2,3-d]pyrimidin-7-one
https://huagongshe.com/ko/reaction/3188
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-(3-Aminopropyl)morpholine | HCID 61055 | — |
| 반응물 | 6-(2,6-Dichlorophenyl)-8-methyl-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one | HCID 10736701 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 6-(2,6-dichlorophenyl)-8-methyl-2-{[3-(morpholin-4-yl)propyl]amino}-7H,8H-pyrido[2,3-d]pyrimidin-7-one | HCID 5327877 | — |
반응 단계
A mixture of 0.165 g (0.47 mmol) of 6-(2,6-dichlorophenyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 37, 1.00 g (6.90 mmol) of N-(3-aminopropyl)morpholine and 0.5 mL of dimethylformamide was heated with stirring in a 125° C. oil bath. After 2 minutes, solution was complete. After 1.5 hours, the excess amine and dimethylformamide were evaporated at reduced pressure and the residue was triturated with 5 mL of water. The gum was dissolved in 25 mL of ethyl acetate, and the solution was washed with 2×5 mL of water, dried (potassium carbonate), and concentrated. Upon dissolution in 5 mL of ether, crystals of pure product separated; wt 0.101 g; mp 140°-142° 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-ed41f375aaff41018a80d7b0ecb415a0 |
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| 출처 메모 | uspto-grants-1998_03 |
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