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HRID 1472739作成日:2026年10月25日

Ammonium formate → (R)-5-(2-Amino-1-(tert-butyldimethylsilyloxy)ethyl)-8-hydroxyquinolin-2(1H)-one formate

https://huagongshe.com/reaction/1472739

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium formateHCID 2723923—
反応物(R)-5-(2-Azido-1-((tert-butyldimethylsilyl)oxy)ethyl)-8-(benzyloxy)quinolin-2(1H)-oneHCID 58505233—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物(R)-5-(2-Amino-1-(tert-butyldimethylsilyloxy)ethyl)-8-hydroxyquinolin-2(1H)-one formateHCID 7109330286%

反応条件

温度80 °C

反応手順

Palladium on activated carbon (0.4 g, 10% w/w) was added to a suspension of (R)-5-(2-azido-1-(tert-butyldimethylsilyloxy)ethyl)-8-(benzyloxy)quinolin-2(1H)-one (2.05 g, 4.60 mmol) and ammonium formate (2.87 g, 63 mmol) in methanol (50 mL). The reaction mixture was heated at 80° C. for 1 hour and then filtered through celite, washing with water. The reaction mixture was concentrated under reduced pressure. The resultant solid was washed with water, triturated with ethyl acetate and collected by filtration to afford the title compound (1.32 g, 86%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09012644B2
出典データセットuspto-grants-2015_04
ORD IDord-aa4cb0be25d14da4abf8ca9ec63e4b7b
出典メモuspto-grants-2015_04