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HRID 324778作成日:2026年10月26日

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

https://huagongshe.com/reaction/324778

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-DichlorobenzaldehydeHCID 22710—
反応物Sodium AcetateHCID 517045—
反応物Pyridine-4-amidine hydrochlorideHCID 2776844—
反応物3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetateHCID 22005512—
溶媒DimethylformamideHCID 6228—
生成物3-Phenylpropyl 4-(3,4-dichlorophenyl)-6-[(2-(1-piperidinyl)ethoxy)methyl]-2-(4-pyridyl)-1,4-dihydropyrimidine-5-carboxylateHCID 220055313.1%

反応条件

温度60 °C

反応手順

A mixture of 3-phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate (1.50 g, 4.32 mmol), 3,4-dichlorobenzaldehyde (0.907 g, 5.18 mmol), 4-amidinopyridine hydrochloride (0.816 g, 5.18 mmol) and sodium acetate (0.425 g, 5.18 mmol) was stirred in N,N-dimethylformamide (10 mL) for 14 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 to give the title compound (81.7 mg) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06218538B1
出典データセットuspto-grants-2001_04
ORD IDord-76d939b350284a8cb06b7161a68ee743
出典メモuspto-grants-2001_04