戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 448571作成日:2026年10月25日

Cesium carbonate → 4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-5-methoxy-pyrimidin-4-yloxy]-piperidine-1-carboxylic acid isopropyl ester

https://huagongshe.com/reaction/448571

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Tri-tert-butylphosphine tetrafluoroborateHCID 2734635—
反応物5-(Methanesulfonyl)-2,3-dihydro-1H-indoleHCID 2736136—
反応物Isopropyl 4-[(6-chloro-5-methoxypyrimidin-4-yl)oxy]piperidine-1-carboxylateHCID 51050526—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒1,4-DioxaneHCID 31275—
生成物4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-5-methoxy-pyrimidin-4-yloxy]-piperidine-1-carboxylic acid isopropyl esterHCID 25261148—

反応条件

温度90 °C

反応手順

A mixture of 8a (49 mg, 0.15 mmol), cesium carbonate (0.11 g, 2 eq), 5-Methanesulfonyl-2,3-dihydro-1H-indole (35 mg, 1.2 eq), tris(dibenzylideneacetone)-dipalladium (31 mg, 0.1 eq), tri-t-butylphosphonium tetrafluoroborate (37 mg, 0.8 eq) and dioxane (1.5 mL) was heated at 90° C. for 4 h. The mixture cooled to room temperature, dioxane was added and the mixture was filtered and washed with DCM. The filtrate was concentrated under a stream of nitrogen and the residue was taken up in 1 mL of THF and was purified by preparative HPLC to afford 8-1; LCMS 491.2 (MH+), tR=5.35 (Method 6). EC50: 201 nM.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481731B2
出典データセットuspto-grants-2013_07
ORD IDord-653be0dfc5924825b24740bb09feb911
出典メモuspto-grants-2013_07