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HRID 216122作成日:2026年10月25日

2-Methyl-2-butene → 2-Fluoro-5-{2-methoxy-6-[2-(4-methoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzoic acid

https://huagongshe.com/reaction/216122

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-2-buteneHCID 10553—
反応物Sodium Phosphate, Monobasic, MonohydrateHCID 516949—
反応物2-Fluoro-5-{2-methoxy-6-[2-(4-methoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzaldehydeHCID 11581719—
反応物Sodium ChloriteHCID 23668197—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
溶媒TetrahydrofuranHCID 8028—
生成物2-Fluoro-5-{2-methoxy-6-[2-(4-methoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzoic acidHCID 11696919—

反応手順

A solution of 2-fluoro-5-{2-methoxy-6-[2-(4-methoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzaldehyde [120 mg, 0.31 mmol, Example 35(j)] and 2-methyl-2-butene (2.93 mL, 28 mmol) in t-butanol (4 mL) and THF (2 mL), is treated with a solution of sodium dihydrogen phosphate monohydrate (303 mg, 2.2 mmol) and sodium chlorite (0.28 g, 3.2 mmol) in water (2 mL) at room temperature. After 15 hours at 20° C., the mixture is concentrated and diluted with water. The mixture is adjusted to pH 3 and the resulting solid is filtered and dried to afford 2-fluoro-5-{2-methoxy-6-[2-(4-methoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzoic acid. [118 mg, 96%, Example 20(a)]. LCMS: RT=2.38 minutes, MS: 398 (M+H). IC50=0.4 nM

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193183B2
出典データセットuspto-grants-2012_06
ORD IDord-c165c3a0ebfe433a97186adc2a99ef27
出典メモuspto-grants-2012_06