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HRID 2172014作成日:2026年10月24日

1-(Pyrimidin-2-yl)propan-2-one → (E)-N-(1-benzhydrylazetidin-3-yl)oxy-1-pyrimidin-2-ylpropan-2-imine

https://huagongshe.com/ja/reaction/2172014

反応式

関与物質

役割名称HCID仕込み量
反応物1-(Pyrimidin-2-yl)propan-2-oneHCID 12656663—
反応物3-(Aminooxy)-1-(diphenylmethyl)azetidineHCID 67154688—
溶媒EthanolHCID 702—
生成物(E)-N-(1-benzhydrylazetidin-3-yl)oxy-1-pyrimidin-2-ylpropan-2-imineHCID 88941950100.7%

反応手順

A solution of 1-pyrimidin-2-ylacetone (27 mg, 0.2 mmol; which may be prepared as described in Step 1) and 3-(aminooxy)-1-(diphenylmethyl)azetidine (51 mg, 0.2 mmol; which may be prepared as described in Step 3) in ethanol (2 mL) under nitrogen was stirred at 80° C. overnight. The crude mixture was concentrated to dryness to give the title compound (75 mg, quantitative) as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09051321B2
出典データセットuspto-grants-2015_06
ORD IDord-00e2ed0eeca3486fad70fadbefde5f72
出典メモuspto-grants-2015_06