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HRID 1931686作成日:2026年10月26日

Potassium Carbonate → 4-[4-(4-[1,2,4]Triazol-1-yl-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1931686

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-(1,2,4-Triazol-1-yl)phenolHCID 110064—
反応物Tert-butyl 4-(4-chloro-1H-pyrazolo[3,4-D]pyrimidin-1-YL)piperidine-1-carboxylateHCID 57964905—
溶媒DimethylformamideHCID 6228—
生成物4-[4-(4-[1,2,4]Triazol-1-yl-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 5325791542%

反応条件

温度180 °C

反応手順

A mixture of 4-(1,2,4)-triazol-1-yl-phenol (Lancaster; 14 mg, 0.09 mmol), 4-(4-chloro-pyrazolo[3,4-d]pyrimidin-1-yl)-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 19; 29.5 mg, 0.09 mmol) and potassium carbonate (14.4 mg, 0.10 mmol) in anhydrous DMF (1 mL) was heated in a microwave at 180° C. for 10 min. The mixture was cooled and filtered. The solid was washed with dichloromethane. The filtrate was concentrated and purified using a 4 g silica gel column, eluting with 0-5% methanol/dichloromethane to give 4-[4-(4-[1,2,4]triazol-1-yl-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester (17 mg, 42%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08188098B2
出典データセットuspto-grants-2012_05
ORD IDord-2083c48bac7b4ee094522fe1376e1d39
出典メモuspto-grants-2012_05