戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 403497作成日:2026年10月25日

Propane, 1,1-diethoxy- → 3-[4-(4-Diethoxymethyl-[1,2,3]triazol-1-yl)-benzyl]-2-ethyl-5,7-dimethyl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/403497

反応式

関与物質

役割名称HCID仕込み量
反応物Propane, 1,1-diethoxy-HCID 20858—
反応物HCID 86671756HCID 86671756—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物3-[4-(4-Diethoxymethyl-[1,2,3]triazol-1-yl)-benzyl]-2-ethyl-5,7-dimethyl-pyrazolo[1,5-a]pyrimidineHCID 68378910—

反応手順

A solution of 3-(4-azido-benzyl)-2-ethyl-5,7-dimethyl-pyrazolo[1,5-a]pyrimidine (20) (2 g, 6.53 mmol), propionaldehyde diethylacetal (1.294 g, 9.79 mmol) and copper(I) iodide (1.492 g, 7.83 mmol) in 33 ml of acetonitrile was stirred at r.t. for 24 h. The reaction was diluted in EtOAc and washed with sat aq Na2 CO3, water and brine. The organic layer was dried over anhydrous Na2 SO4, filtered and concentrated under HV. The crude product was purified by flash chromatography (silica gel, EtOAc/DCM 0% to 50%) to give a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748435B2
出典データセットuspto-grants-2014_06
ORD IDord-e4fa77d7e9774dbaadf070dc482553ab
出典メモuspto-grants-2014_06