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HRID 448585作成日:2026年10月26日

Diisopropylethylamine → 4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-pyrimidin-4-ylamino]-piperidine-1-carboxylic acid isopropyl ester

https://huagongshe.com/reaction/448585

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Isopropyl 4-aminopiperidine-1-carboxylateHCID 46941577—
反応物1-(6-Chloropyrimidin-4-yl)-5-(methylsulfonyl)indolineHCID 59566526—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-pyrimidin-4-ylamino]-piperidine-1-carboxylic acid isopropyl esterHCID 4984878514%

反応条件

温度90 °C

反応手順

A mixture of 18b (1.1 g, 5.9 mmol), 6a (1.5 g, 4.84 mmol) and diisopropylethylamine (3 mL, 18.1 mmol) in 15 mL of DMF was heated at 80° C. for 17 h and at 90° C. for 24 h. The mixture was diluted with 100 mL of DCM, washed with brine (3×50 mL) and the extracts were dried, filtered and concentrated under vacuum. The residue was purified by flash chromatography (elution with 50-100% ethyl acetate and 0.1% TEA in hexanes) and finally purified on preparative HPLC to afford 0.3 g (14%) of 18-1. tR=5.21 (Method 5). EC50: 611 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-93eb12c28a2d44f993aaf834adfc9f75
出典メモuspto-grants-2013_07