Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2233213생성일: 2026년 10월 25일
Methanol → Ethyl 3-{4-hydroxy-6-oxo-2-[(E)-2-phenylethenyl]-1,6-dihydro-5-pyrimidinyl}propanoate
https://huagongshe.com/reaction/2233213
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 3-Ethyl 1,1-dimethyl 1,1,3-propanetricarboxylate | HCID 13042480 | — |
| 반응물 | Cinnamimidamide | HCID 14668188 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Ethyl 3-{4-hydroxy-6-oxo-2-[(E)-2-phenylethenyl]-1,6-dihydro-5-pyrimidinyl}propanoate | HCID 67548308 | — |
반응 단계
3-Ethyl 1,1-dimethyl 1,1,3-propanetricarboxylate (1.65 g, 7.11 mmol) and (2E)-3-phenyl-2-propenimidamide (1.04 g, 7.11 mmol) were combined in EtOH (36 mL). Triethylamine (1.98 mL, 14.2 mmol) was added and the solution was heated at reflux for 3 h with no change based on LCMS. The solution was cooled to room temperature and treated with NaOMe in MeOH (1.0 mL, 5.33 mmol, 25% wt solution) and the solution was refluxed for an additional 4 h. Another portion of NaOMe in MeOH (1.0 mL, 5.33 mmol, 25% wt solution) was added and the solution was refluxed for 16 h. After this time, a yellow precipitate had formed which was filtered off. The mother liquor was acidified to pH2 with 1N HCl, and the solution was concentrated under vacuum. The resulting material was combined with the yellow solid and used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07709483B2 |
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| 출처 데이터셋 | uspto-grants-2010_05 |
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| ORD ID | ord-d00b5518438f4d2a9aa5e8bfe439c582 |
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| 출처 메모 | uspto-grants-2010_05 |
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