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HRID 1453865作成日:2026年10月27日

Cesium carbonate → Dimethyl 4-benzyloxy-1-(3-bromopropyl)-1H-pyrazole-3,5-dicarboxylate

https://huagongshe.com/reaction/1453865

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2,2-DibromopropaneHCID 11658—
反応物dimethyl 4-benzyloxy-1H-pyrazole-3,5-dicarboxylateHCID 57528491—
溶媒DimethylformamideHCID 6228—
生成物Dimethyl 4-benzyloxy-1-(3-bromopropyl)-1H-pyrazole-3,5-dicarboxylateHCID 69080907—

反応手順

To a solution of dimethyl 4-benzyloxy-1H-pyrazole-3,5-dicarboxylate (200 mg, 0.689 mmol) in DMF (3 mL) under an atmosphere of nitrogen at 0° C. was added dibromopropane (211 μL, 2.067 mmol) and Cs2CO3 (269 mg, 0.827 mmol). The ice bath was removed, and the reaction was stirred at room temperature overnight. The solvent was removed in vacuo, and the resulting residue was partitioned between EtOAc and water. The aqueous layer was extracted into EtOAc once, and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated in vacuo. the residue was purified by flash column chromatography on silica gel using a 0-50% EtOAc/hexanes gradient elution. Collection and concentration of the appropriate fractions afforded the compound. 1H NMR (400 MHz, CDCl3) δ 7.47-7.44 (m, 2H), 7.40-7.34 (m, 3M), 5.13 (s, 2H), 4.71-4.67 (t, 2H), 3.96 (s, 3H), 3.87 (s, 3H), 3.39-3.36 (t, 2H), 2.45-2.38 (dt, 2H); ES MS (M+1)=412.

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-23e4a8f716d14da49f8053f2daa917f6
出典メモuspto-grants-2009_01