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HRID 524589作成日:2026年10月27日

Potassium Carbonate → Ethyl 4-(2-bromo-4-fluorophenyl)-6-((3-carbamoylmorpholino) methyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate

https://huagongshe.com/reaction/524589

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Morpholine-3-carboxamideHCID 19792002—
反応物Ethyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 59495567—
溶媒EthanolHCID 702—
生成物Ethyl 4-(2-bromo-4-fluorophenyl)-6-((3-carbamoylmorpholino) methyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylateHCID 7329494850.1%

反応条件

温度25 °C

反応手順

A mixture of ethyl 4-(2-bromo-4-fluorophenyl)-6-(bromomethyl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (3.02 g, 6 mmol), morpholine-3-carboxamide (0.78 g, 6 mmol) and potassium carbonate (1.66 g, 12 mmol) in anhydrous ethanol (70 mL) was stirred at 25° C. for 12 hours under N2. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by a silica gel column chromatography (DCM/MeOH (V/V)=100/1) to give the title compound as a yellow solid (1.66 g, 50%). The compound was characterized by the following spectroscopic data:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09340538B2
出典データセットuspto-grants-2016_05
ORD IDord-21d4a092be1f4a46a5785bf4e7e8bc9e
出典メモuspto-grants-2016_05