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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400995생성일: 2026년 10월 24일

Hydrochloric Acid → 4-(3-ethoxy-4-hydroxy-5-nitrophenyl)-6-phenyl-5-(thiazol-2-yl)-3,4-dihydropyrimidin-2(1H)-one

https://huagongshe.com/ko/reaction/400995

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물UreaHCID 1176—
반응물3-Ethoxy-4-hydroxy-5-nitrobenzaldehydeHCID 584878—
반응물1-Phenyl-2-(thiazol-2-yl)ethanoneHCID 17887047—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물4-(3-ethoxy-4-hydroxy-5-nitrophenyl)-6-phenyl-5-(thiazol-2-yl)-3,4-dihydropyrimidin-2(1H)-oneHCID 569613443.4%

반응 단계

To a mixture of 1-phenyl-2-(thiazol-2-yl)ethanone (Intermediate 3) (170 mg, 0.84 mmol), 3-ethoxy-4-hydroxy-5-nitrobenzaldehyde (212 mg, 1.00 mmol), and urea (151 mg, 2.52 mmol) in anhydrous EtOH (20 mL) was added concentrated HCl solution (0.1 mL), and the reaction mixture was refluxed for three days. When TLC (EtOAc:MeOH=10:1) showed that about 30% of the starting materials were consumed, the reaction mixture was concentrated, and the crude product was purified by column chromatography and preparative HPLC to afford Compound 12 as a yellow solid (12.5 mg, yield: 3.4%). 1H NMR (DMSO-d6 400 MHz TMS): δ 10.25 (s, 1H), 9.25 (s, 1H), 7.82 (s, 1H), 7.50-7.56 (m, 4H), 7.48 (s, 1H), 7.36-7.40 (m, 3H), 7.22 (d, J=3.6 Hz, 1H), 5.68 (d, J=3.6 Hz, 1H), 4.10 (q, J=6.0 Hz, 2H), 1.35 (t, J=7.2 Hz, 3H); MS (ESI): m/z 439.1 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741915B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-06927dcb77ee425d8e18d68f1b721b09
출처 메모uspto-grants-2014_06