Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1468779생성일: 2026년 10월 26일
Potassium Carbonate → 2-[4-(1-Methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yloxy)piperidin-1-yl]benzaldehyde
https://huagongshe.com/reaction/1468779
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | o-Fluorobenzaldehyde | HCID 67970 | — |
| 반응물 | 1-methyl-2-(piperidin-4-yloxy)-1H-[4,4']bipyrimidinyl-6-one | HCID 67977650 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | 2-[4-(1-Methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yloxy)piperidin-1-yl]benzaldehyde | HCID 86669146 | 52.3% |
반응 단계
To a mixture of 1-methyl-2-(piperidin-4-yloxy)-1H-[4,4′]bipyrimidinyl-6-one (1.00 g, 3.48 mmol) and 2-fluorobenzaldehyde (475 mg, 3.83 mmol) in dimethyl sulfoxide (3.50 ml) was added potassium carbonate (1.44 g, 10.4 mmol). The mixture was stirred at 120° C. for 4 hours. The mixture was partitioned between water and chloroform. The organic layer was washed with water (three times), dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (eluent; ethyl acetate) to afford 2-[4-(1-methyl-6-oxo-1,6-dihydro-[4,4′]bipyrimidinyl-2-yloxy)piperidin-1-yl]benzaldehyde as a yellow solid (711 mg, 1.82 mmol, 52%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09006232B2 |
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| 출처 데이터셋 | uspto-grants-2015_04 |
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| ORD ID | ord-0fee3f999b644fa2b2ef5dd27ce5ed67 |
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| 출처 메모 | uspto-grants-2015_04 |
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