戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1020816作成日:2026年10月27日

Water → 5-Chloro-6-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-(4-oxohexyloxy)nicotinonitrile

https://huagongshe.com/reaction/1020816

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Cesium carbonateHCID 10796—
反応物1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-olHCID 57968699—
反応物1-(3-(5,6-Dichloro-3-cyanopyridin-2-yloxy)propyl)cyclopropyl 2,2,2-trifluoroacetateHCID 86661725—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
生成物5-Chloro-6-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-(4-oxohexyloxy)nicotinonitrileHCID 58080030—

反応条件

温度40 °C

反応手順

To a mixture of compound 1-(3-(5,6-dichloro-3-cyanopyridin-2-yloxy)propyl)cyclopropyl 2,2,2-trifluoroacetate (0.87 g, 2.3 mmol) and benzo[c][1,2]oxaborole-1,5(3H)-diol (0.36 g, 2.4 mmol) in DMSO was added Cs2CO3 (0.89 g, 2.7 mmol) at room temperature and the resulting mixture was stirred at 40° C. overnight. The mixture was then poured into cold water, diluted with EtOAc, the organic phase was separated and the aqueous phase was further extracted twice with EtOAc. The combined organic layers were washed with brine twice, dried over Na2SO4 and concentrated, the residue was purified by Prep-HPLC (column: Luna 300×50.0 mm, 10μ; liquid phase: [A-H2O; B—CH3CN] B %: 35%-62%, 23 min) to give the product D233 (105 mg) and D234 (112 mg), total yield 24%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08716478B2
出典データセットuspto-grants-2014_05
ORD IDord-616d124f5c65419ca086c4a0634e36f5
出典メモuspto-grants-2014_05