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HRID 350912作成日:2026年10月25日

Dichloroacetic Acid → 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-4-methylbenzoic acid

https://huagongshe.com/reaction/350912

反応式

関与物質

役割名称HCID仕込み量
反応物Dichloroacetic AcidHCID 6597—
反応物ChlorosuccinimideHCID 31398—
反応物3-[4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-4-methylbenzoic acidHCID 21088985—
溶媒1,1-DichloroethaneHCID 6365—
生成物3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-4-methylbenzoic acidHCID 2108930648%

反応条件

温度65 °C

反応手順

3-[4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-4-methylbenzoic acid (from Step 2) (6.62 g, 17.8 mmol), N-chlorosuccinimide (2.85 g, 21.3 mmol), and dichloroacetic acid (4 mL) are combined in dichloroethane (50 mL) and heated at 65° C. for 65 h. The reaction mixture is cooled to 0° C. and the precipitate is filtered, washed with cold dichloroethane, and dried in vacuo. Product obtained as a white solid (3.47 g, 48%). Used without further purification. 1H NMR (CD3OD/300 MHz) δ8.32 (s, 1H), 8.09 (m, 1H), 7.94 (s, 1H), 7.62 (q, 1H, J=8.4 Hz), 7.54 (d, 1H, J=7.8 Hz), 7.03 (m, 2H), 5.61 (s, 2H), 2.21 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07183287B2
出典データセットuspto-grants-2007_02
ORD IDord-f713496bcb26407b8b8a6c757e7fad3c
出典メモuspto-grants-2007_02