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HRID 1409739作成日:2026年10月26日

Tetrapropylammonium → 1-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidin-4-one

https://huagongshe.com/reaction/1409739

反応式

関与物質

役割名称HCID仕込み量
反応物TetrapropylammoniumHCID 9559—
反応物Methyl morpholine oxideHCID 82029—
反応物1-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidin-4-OLHCID 21897744—
溶媒DichloromethaneHCID 6344—
生成物1-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidin-4-oneHCID 66915348—

反応手順

1-[3-(Propan-2-yl)-1,2,4-oxadiazol-5-yl]piperidin-4-ol (0.5 g) is dissolved in dichloromethane (75 mL) and 4 A molecular sieves (4 g) are added followed by N-methylmorpholine-N-oxide (1.52 g) and tetrapropylammonium perrhutenate (0.018 g) and the mixture is stirred at room temperature for 1 h. The reaction is then filtered through celite and the mother liquor washed with water (2×50 mL). The water layers are then combined and back extracted with dichloroemthane (100 mL). The dichloromethane layers are combined, dried over Na2SO4, filtered and concentrated to give the title compound. LC (method 20): tR=1.67 min; Mass spectrum (APCI): m/z=210 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921398B2
出典データセットuspto-grants-2014_12
ORD IDord-38fbc51127124e7badac6fcceb6e2ec6
出典メモuspto-grants-2014_12