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HRID 1688565作成日:2026年10月27日

Tetrahydrofuran → HCID 178438685、化合物

https://huagongshe.com/reaction/1688565

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物4'-({5-oxo-7-propyl-4-[(3a'R,6a'S)-tetrahydro-3a'H-spiro[cyclohexane-1,2'-cyclopenta[d][1,3]dioxol]-4-yl]-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrileHCID 67009097—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 178438685HCID 17843868572%

反応条件

温度70 °C

反応手順

A mixture of 4′-({5-oxo-7-propyl-4-[(3a′R,6a′S)-tetrahydro-3a′H-spiro[cyclohexane-1,2′-cyclopenta[d][1,3]dioxol]-4-yl]-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (1.2 g), sodium cyanoborohydride (0.65 g), boron trifluoride-diethyl ether complex (1.3 mL) and tetrahydrofuran (30 mL) was stirred at 70° C. for 16 hr. The reaction mixture was diluted with ethyl acetate, washed with water and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.82 g, 72%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08148383B2
出典データセットuspto-grants-2012_04
ORD IDord-fdc368e7b44a4a67af5cb8e1cf3fb5b0
出典メモuspto-grants-2012_04