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HRID 451412作成日:2026年10月27日

Diisopropylethylamine → tert-butyl N-[1-(6-methylpyrimidin-4-yl)piperidin-4-yl]carbamate

https://huagongshe.com/reaction/451412

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4-Chloro-6-methylpyrimidineHCID 581796—
反応物4-Amino-1-Boc-piperidineHCID 1268291—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物tert-butyl N-[1-(6-methylpyrimidin-4-yl)piperidin-4-yl]carbamateHCID 67343276—

反応条件

温度150 °C

反応手順

A suspension of Boc-4-aminopiperidine (613 mg, 3 mmol), 4-chloro-6-methylpyrimidine (433 mg, 3.3 mmol) and N,N-diisopropylethyl amine (771 L, 4.5 mmol) in dioxane (12 mL) was heated to 150° C. in the microwave for 30 minutes. The reaction was diluted with water and extracted twice with ethyl acetate. The combined organic layers were washed with water, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel using a gradient from AcOEt to AcOEt/EtOH 9:1 as eluent. The title compound was obtained as a light yellow solid (693 mg, 79%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08486967B2
出典データセットuspto-grants-2013_07
ORD IDord-6de883d95cf14582bc0237df04c0840d
出典メモuspto-grants-2013_07