Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 872300생성일: 2026년 10월 25일
Triethylamine → 5-[4-(7-Methoxy-3-phenyl-imidazo[1,2-a]pyrimidin-2-yl)-phenyl]-2-oxa-4-aza-bicyclo[3.1.1]heptan-3-one
https://huagongshe.com/reaction/872300
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Methoxy-2-pyrimidinamine | HCID 67428 | — |
| 반응물 | 5-[4-(2-Bromo-2-phenyl-acetyl)-phenyl]-2-oxa-4-aza-bicyclo[3.1.1]heptan-3-one | HCID 86691039 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 5-[4-(7-Methoxy-3-phenyl-imidazo[1,2-a]pyrimidin-2-yl)-phenyl]-2-oxa-4-aza-bicyclo[3.1.1]heptan-3-one | HCID 66665118 | — |
반응 단계
A mixture of crude 5-[4-(2-bromo-2-phenyl-acetyl)-phenyl]-2-oxa-4-aza-bicyclo[3.1.1]heptan-3-one (2.5 g), 4-methoxypyrimidin-2-amine (1.26 g), triethylamine (0.84 mL) and ethanol (62 mL), under argon, was heated at 100° C. (bath temperature) for 6 hours. On cooling the reaction was concentrated and partitioned between EtOAc and water. The aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried and concentrated. Purification was achieved by chromatography on silica gel followed by preparative reverse phase HPLC to give the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08975265B2 |
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| 출처 데이터셋 | uspto-grants-2015_03 |
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| ORD ID | ord-b35483ed864f417a9415f319200dab38 |
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| 출처 메모 | uspto-grants-2015_03 |
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