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HRID 31407作成日:2026年10月24日

Dimethylamine → [5-(4-Iodophenyl)-[1,3,4]oxadiazol-2-ylmethyl]-dimethylamine

https://huagongshe.com/ja/reaction/31407

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物Potassium IodideHCID 4875—
反応物2-(Chloromethyl)-5-(4-iodophenyl)-1,3,4-oxadiazoleHCID 7091068—
溶媒TetrahydrofuranHCID 8028—
生成物[5-(4-Iodophenyl)-[1,3,4]oxadiazol-2-ylmethyl]-dimethylamineHCID 69314787—

反応条件

温度20 °C

反応手順

2-Chloromethyl-5-(4-iodophenyl)-[1,3,4]oxadiazole (Intermediate 7) (48 mg, 0.15 mmol) and potassium iodide (25 mg, 0.15 mmol) were dissolved in 2M dimethylamine in tetrahydrofuran (2 ml) and stirred for 18 hours at 20° C. The reaction was evaporated to dryness in vacuo and the product was purified on a 10 g silica SPE cartridge (stepped solvent gradient 80:20 ethyl acetate:cyclohexane, 100% ethyl acetate, 95:5 ethyl acetate:methanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425555B2
出典データセットuspto-grants-2008_09
ORD IDord-c2559fa983e245c3a7bffa15abcab064
出典メモuspto-grants-2008_09