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HRID 38873作成日:2026年10月24日

Cyclohexanemethanol → {5-[6-(1H-Indol-4-yl)-1H-indazol-4-yl]-1,3,4-oxadiazol-2-yl}methanol

https://huagongshe.com/ja/reaction/38873

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexanemethanolHCID 7507—
反応物Potassium CarbonateHCID 11430—
反応物4-[5-(Chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazoleHCID 66776954—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物{5-[6-(1H-Indol-4-yl)-1H-indazol-4-yl]-1,3,4-oxadiazol-2-yl}methanolHCID 6669192229.6%

反応条件

温度100 °C

反応手順

4-[5-(Chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazole (25 mg, 0.051 mmol), cyclohexylmethanol (17.48 mg, 0.153 mmol) and potassium carbonate (21.16 mg, 0.153 mmol) were placed in N-methyl-2-pyrrolidone (1 ml) and the mixture heated under microwave irradiation at 100° C. for 20 mins. Additional cyclohexylmethanol (17.48 mg, 0.153 mmol) was added and the mixture heated at 110° C. for 20 mins, followed by 110° C. for a further 20 mins. The solvent was removed and the residue purified by Mass Directed Automated Preparative HPLC to give the title compound as a white solid (5 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524751B2
出典データセットuspto-grants-2013_09
ORD IDord-a8aed5489aee458d9214f40f1d9238cf
出典メモuspto-grants-2013_09