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HRID 75415作成日:2026年10月25日

3-[6-Chloro-2-(4-nitro-phenyl)-pyrimidin-4-yl]-8-oxa-3-aza-bicyclo[3.2.1]octane → Isopropyl-[2-(4-nitro-phenyl)-6-(8-oxa-3-aza-bicyclo[3.2.1]oct-3-yl)-pyrimidin-4-yl]-amine

https://huagongshe.com/reaction/75415

反応式

関与物質

役割名称HCID仕込み量
反応物3-[6-Chloro-2-(4-nitro-phenyl)-pyrimidin-4-yl]-8-oxa-3-aza-bicyclo[3.2.1]octaneHCID 86665884—
溶媒IsopropylamineHCID 6363—
生成物Isopropyl-[2-(4-nitro-phenyl)-6-(8-oxa-3-aza-bicyclo[3.2.1]oct-3-yl)-pyrimidin-4-yl]-amineHCID 66750217198.3%

反応条件

温度140 °C

反応手順

In a 2-5 mL microwave vial was placed 3-(6-chloro-2-(4-nitrophenyl)pyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octane (13, 70 mg, 0.202 mmol) in iPrNH2 (4 ml) to give a yellow suspension. The reaction was heated under microwave irradiation at 140° C. for 90 min. The mixture was concentrated, dissolved in dichloromethane and washed with sat NaHCO3. The organic phase was dried over MgSO4, filtered and concentrated to give 74 mg of the title compound as a yellow solid (99%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835429B2
出典データセットuspto-grants-2014_09
ORD IDord-fbe7ae7ed2ba4f29b4669ac13aad8e01
出典メモuspto-grants-2014_09