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HRID 1409099作成日:2026年10月25日

Sodium Iodide → HCID 178505979、化合物

https://huagongshe.com/reaction/1409099

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Isoamyl NitriteHCID 8053—
反応物HCID 178509230HCID 178509230—
溶媒AcetoneHCID 180—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178505979HCID 178505979—

反応条件

温度0 °C

反応手順

10 g (65.75 mmol) of 5-fluoro-1H-pyrazolo[3,4-b]pyridine-3-amine were initially charged in THF (329 ml), and the mixture was cooled to 0° C. 16.65 ml (131.46 mmol) of boron trifluoride diethyl ether complex were then added slowly. The reaction mixture was cooled further to −10° C. A solution of 10.01 g (85.45 mmol) of isopentyl nitrite in THF (24.39 ml) was then added slowly, and the mixture was stirred for a further 30 min. The mixture was diluted with cold diethyl ether (329 ml) and the resulting solid was isolated by filtration. A little at a time, the diazonium salt thus prepared was added to a cold (0° C.) solution of 12.81 g (85.45 mmol) of sodium iodide in acetone (329 ml), and the mixture was stirred at RT for 30 min. The reaction mixture was poured into ice-water (1.8 l) and extracted twice with ethyl acetate (487 ml each time). The collected organic phases were washed with saturated aqueous sodium chloride solution (244 ml), dried, filtered and concentrated. This gave 12.1 g (86% purity, 60% of theory) of the desired compound in the form of a brown solid. The crude product was reacted without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921377B2
出典データセットuspto-grants-2014_12
ORD IDord-b59f137a7f7a4abe9de334b87ffc10b3
出典メモuspto-grants-2014_12