戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 38845作成日:2026年10月24日

Sodium Iodide → N-{[5-(6-Bromo-1H-indazol-4-yl)-1,3,4-oxadiazol-2-yl]methyl}-3-(4-morpholinyl)-1-propanamine

https://huagongshe.com/ja/reaction/38845

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物N-(3-Aminopropyl)morpholineHCID 61055—
反応物DiisopropylethylamineHCID 81531—
反応物6-bromo-4-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-1-(phenylsulfonyl)-1H-indazoleHCID 66695668—
溶媒AcetonitrileHCID 6342—
生成物N-{[5-(6-Bromo-1H-indazol-4-yl)-1,3,4-oxadiazol-2-yl]methyl}-3-(4-morpholinyl)-1-propanamineHCID 66693558117.8%

反応条件

温度70 °C

反応手順

6-Bromo-4-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-1-(phenylsulfonyl)-1H-indazole (300 mg, 0.661 mmol) and sodium iodide (99 mg, 0.661 mmol) were weighed into a round-bottomed flask and dissolved in acetonitrile (2 ml) before [3-(4-morpholinyl)propyl]amine (191 mg, 1.322 mmol, available from Sigma-Aldrich) and DIPEA (0.231 ml, 1.322 mmol) were added. The mixture was heated to 70° C. for 2 h, then cooled and the solvent removed under a stream of nitrogen. The crude residue was dissolved in DCM/MeOH (1:1) and preadsorbed onto silica which was then added to the top of a 20 g silica cartridge that was subsequently eluted with 0-15% MeOH(+1% triethylamine)/DCM over 20 mins. The appropriate fractions were combined and the solvent removed in vacuo to give the title compound as a yellow oily solid (328 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-efdc4be0799741cea96b3527d01e17f1
出典メモuspto-grants-2013_09