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HRID 2355941作成日:2026年10月27日

3,4-dihydro-6-hydroxy-3-(1-phenylmethyl-4-piperidinyl)-2(1H)-quinazolinone → 6-Hydroxy-3-piperidin-4-yl-3,4-dihydro-1H-quinazolin-2-one

https://huagongshe.com/reaction/2355941

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-dihydro-6-hydroxy-3-(1-phenylmethyl-4-piperidinyl)-2(1H)-quinazolinoneHCID 17958692—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物6-Hydroxy-3-piperidin-4-yl-3,4-dihydro-1H-quinazolin-2-oneHCID 2110220781%

反応手順

3-(1-Benzyl-piperidin-4-yl)-6-hydroxy-3,4-dihydro-1H-quinazolin-2-one (100 mg, 0.3 mmol) in methanol (5 mL) was flushed with nitrogen, and treated with palladium on charcoal (10%, 10 mg). The flask was flushed with hydrogen and allowed to stir under an atmosphere of hydrogen overnight. The reaction was flushed with nitrogen, filtered through celite, and concentrated. Column chromatography gave 60 mg (81%) of the desired material. LC/MS: tR=0.75 min, 248.22 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07754732B2
出典データセットuspto-grants-2010_07
ORD IDord-645f24b45b0d45339a88e1c863d5f68c
出典メモuspto-grants-2010_07