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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324777생성일: 2026년 10월 27일

3,4-Dichlorobenzaldehyde → 3-Phenylpropyl 4-(3,4-dichlorophenyl)-2-(2-furyl)-6-[(2-(1-piperidinyl)ethoxy)methyl]-1,4-dihydropyrimidine-5-carboxylate

https://huagongshe.com/reaction/324777

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참여 물질

역할이름HCID투입량
반응물3,4-DichlorobenzaldehydeHCID 22710—
반응물Sodium BicarbonateHCID 516892—
반응물Furan-2-carboximidamide hydrochlorideHCID 12231049—
반응물3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetateHCID 22005512—
용매DimethylformamideHCID 6228—
생성물3-Phenylpropyl 4-(3,4-dichlorophenyl)-2-(2-furyl)-6-[(2-(1-piperidinyl)ethoxy)methyl]-1,4-dihydropyrimidine-5-carboxylateHCID 2200551611.2%

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온도60 °C

반응 단계

A mixture of 3-phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate (3.22 g, 9.27 mmol), 3,4-dichlorobenzaldehyde (1.62 g, 9.27 mmol), 2-amidinofuran hydrochloride (1.36 g, 9.27 mmol) and sodium hydrogen carbonate (0.78 g, 9.27 mmol) was stirred in N,N-dimethylformamide (15 mL) for 3 days at room temperature and then heated to 60° C. for 6 days. The DMF was removed in vacuo and ethyl acetate was added to the residue. The precipitate was removed by filtration and the filtrate was washed with water, sodium hydrogen carbonate solution and brine, dried and evaporated to yield an oil. The oil was further purified by flash chromatography and RP-HPLC to give the title compound (617.1 mg) as an oil. Electrospray MS m/z 596/598 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06218538B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-4990e97a05b048ac8d3d47f7728d1c29
출처 메모uspto-grants-2001_04