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HRID 1453825作成日:2026年10月27日

Cesium carbonate → Dimethyl 4-benzyloxy-1-[cyano(phenyl)methyl]-1H-pyrazole-3,5-dicarboxylate

https://huagongshe.com/reaction/1453825

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Bromobenzyl CyanideHCID 22044—
反応物dimethyl 4-benzyloxy-1H-pyrazole-3,5-dicarboxylateHCID 57528491—
溶媒DimethylformamideHCID 6228—
生成物Dimethyl 4-benzyloxy-1-[cyano(phenyl)methyl]-1H-pyrazole-3,5-dicarboxylateHCID 68953781—

反応手順

A solution of dimethyl 4-benzyloxy-1H-pyrazole-3,5-dicarboxylate (1.0 g, 3.45 mmol) and bromo(phenyl)acetonitrile (810 mg, 4.13 mmol) in anhydrous DMF was treated with Cs2CO3 (1.46 g, 4.48 mmol) and stirred at room temperature for 3 days. The solvent was removed in vacuo and the residue was partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc several times, and the combined organic layers were dried over Na2SO4 and concentrated in vacuo. The resulting residue was purified by flash column chromatography on silica gel using a gradient elution of 0-20% EtOAc/hexanes. Collection and concentration of the appropriate fractions yielded the title product as a yellow oil. 1H NMR (400 MHz, d6-DMSO) δ 7.70 (s, 1H), 7.50-7.45 (m, 3H), 7.43-7.29 (m, 7H), 5.08 (s, 2H), 3.86 (s, 3H), 3.81 (s, 3H); ES MS (M+1)=406.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07476666B2
出典データセットuspto-grants-2009_01
ORD IDord-051401307b164482b4af2cae00ad380f
出典メモuspto-grants-2009_01