Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81625생성일: 2026년 10월 26일
Dimethylacetamide → 6-{[5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amine
https://huagongshe.com/reaction/81625
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylacetamide | HCID 31374 | — |
| 반응물 | 4-[(1-Methyl-1H-pyrazol-3-yl)amino]quinazolin-6-ol | HCID 23160382 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | 5-(2,2-Diethoxyethoxy)-2-fluoropyridine | HCID 68429706 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 6-{[5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amine | HCID 68429775 | 65% |
반응 단계
5-(2,2-diethoxyethoxy)-2-fluoropyridine (502 mg, 2.19 mmol) and potassium tert-butoxide (279 mg, 2.49 mmol) were added to an N,N-dimethylacetamide solution (1 ml) of 4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-ol (240 mg, 1.00 mmol), and stirred at 170° C. for 15 hours under a nitrogen atmosphere in a sealed tube. The reaction solution was cooled to room temperature, then water was added, and extracted with chloroform. The organic layer was washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (Biotage, chloroform:methanol=100:3) to obtain 6-{[5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amine (292 mg, yield: 65%) as a brown oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08846700B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-c6d2e65ddbf94c72b551a36e2c02a94f |
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| 출처 메모 | uspto-grants-2014_09 |
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