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HRID 1744306作成日:2026年10月25日

Nitrogen → 5-(2-fluoro-3-methoxyphenyl)-1-[2,6-difluorobenzyl]-3-{3-hydroxy-2(R)-phenylpropyl}-6-methylpyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1744306

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Sodium CarbonateHCID 10340—
反応物2-Fluoro-3-methoxyphenylboronic acidHCID 4985744—
反応物5-bromo-1-[2, 6-difluorobenzyl]-3-{3-acetoxy-2(R)-phenylpropyl}-6-methylpyrimidine-2,4(1H,3H)-dioneHCID 21018399—
溶媒1,4-Dioxane--water (1/1)HCID 21886435—
生成物5-(2-fluoro-3-methoxyphenyl)-1-[2,6-difluorobenzyl]-3-{3-hydroxy-2(R)-phenylpropyl}-6-methylpyrimidine-2,4(1H,3H)-dioneHCID 2101839666.9%

反応手順

To compound 8a (4.05 g, 8 mmol) in dioxane/water (100/50 mL) was added 2-fluoro-3-methoxyphenylboronic acid (2.04 g, 12 mmol) and Na2CO3 (5.08 g, 48 mmol). The reaction mixture was deoxygenated with N2 for 10 min, tetrakis(triphenylphosine) palladium (0) (924 mg, 0.8 mmol) was added and the reaction mixture was heated at 100° C. overnight under the protection of N2. The reaction mixture was partitioned between brine and EtOAc. The organic layer was dried (sodium sulfate), evaporated and purified by flash chromatography (silica, 50% EtOAc/hexanes) to give compound 8b (2.73 g, 66.9%). MS (CI) m/z 511.1 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07015226B2
出典データセットuspto-grants-2006_03
ORD IDord-b9f8959cfd4c47879a75b453e4ca3bfb
出典メモuspto-grants-2006_03