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HRID 1174751作成日:2026年10月25日

2-Fluoro-4-iodoaniline → 4-[6-(2-Fluoro-4-iodo-phenylamino)-5-methyl-pyrimidin-4-yloxy]-piperidine-1-carboxylic Acid Isopropyl Ester

https://huagongshe.com/reaction/1174751

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluoro-4-iodoanilineHCID 185694—
反応物4-(6-Chloro-5-methyl-pyrimidin-4-yloxy)-piperidine-1-carboxylic acid isopropyl esterHCID 11493357—
反応物Sodium t-butoxideHCID 23676156—
触媒palladium(II) acetateHCID 167845—
触媒Biphenyl-3-yl-di-tert-butyl-phosphaneHCID 67201513—
溶媒1,4-DioxaneHCID 31275—
生成物4-[6-(2-Fluoro-4-iodo-phenylamino)-5-methyl-pyrimidin-4-yloxy]-piperidine-1-carboxylic Acid Isopropyl EsterHCID 5985685147.1%

反応条件

温度120 °C

反応手順

A mixture of 4-(6-chloro-5-methyl-pyrimidin-4-yloxy)-piperidine-1-carboxylic acid isopropyl ester (2.58 g, 8.22 mmol), palladium acetate (185 mg, 0.82 mmol), biphenyl-3-yl-di-tert-butyl-phosphane (25 mg, 0.08 mmol), sodium tert-butoxide (2.4 g, 21.2 mmol), and 4-iodo-2-fluoro aniline (2.0 g, 8.4 mmol) in 15 mL dioxane was heated in microwave for 1 hour at 120° C. Solids were filtered off and mixture was purified by column chromatography and precipitating out of hexane/AcOEt to give compound A77 as a tanned solid (1.99 g, 47%). 1H NMR (CDCl3, 400 MHz) δ 1.15-1.16 (d, 6H), 1.61-1.71 (m, 2H), 1.85-1.90 (m, 2H), 1.99 (s, 3H), 3.27-3.33 (m, 2H), 3.63-3.66 (m, 2H), 4.82-4.85 (m, 1H), 5.20-5.23 (m, 1H), 6.35-6.36 (d, 1H), 7.33-7.36 (m, 2H), 8.08-8.13 (m, 1H), 8.22 (s, 1H). Exact mass calculated for C20H24F1N4O3 514.09, found 515.2 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07838525B2
出典データセットuspto-grants-2010_11
ORD IDord-29f4dec8df174ccda5360fe6d91dee17
出典メモuspto-grants-2010_11