Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 657106생성일: 2026년 10월 24일
Triethylamine → Ethyl 3-{4-hydroxy-6-oxo-2-[(E)-2-phenylethenyl]-1,6-dihydro-5-pyrimidinyl}propanoate
https://huagongshe.com/ko/reaction/657106
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 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 | — |
| 용매 | Methanol | HCID 887 | — |
| 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, 25-30% w/w solution) and the solution was refluxed for 3 h. Another two portions of NaOMe in MeOH (2×1.0 mL) were added and the solution was refluxed overnight. After this time, a yellow precipitate had formed which was filtered off. The mother liquor was acidified to pH 2 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 | US08071592B2 |
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| 출처 데이터셋 | uspto-grants-2011_12 |
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| ORD ID | ord-3c93280da30940ca95e13fa68bc03784 |
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| 출처 메모 | uspto-grants-2011_12 |
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