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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

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물TriethylamineHCID 8471—
반응물Sodium MethoxideHCID 10942334—
반응물3-Ethyl 1,1-dimethyl 1,1,3-propanetricarboxylateHCID 13042480—
반응물CinnamimidamideHCID 14668188—
용매EthanolHCID 702—
생성물Ethyl 3-{4-hydroxy-6-oxo-2-[(E)-2-phenylethenyl]-1,6-dihydro-5-pyrimidinyl}propanoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07709483B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-d00b5518438f4d2a9aa5e8bfe439c582
출처 메모uspto-grants-2010_05