戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 74234作成日:2026年10月26日

Phenylacetaldehyde → 5-(Benzoxazol-2-yl)-2-benzyl-1-(tetrahydropyran-4-yl)benzimidazole

https://huagongshe.com/reaction/74234

反応式

関与物質

役割名称HCID仕込み量
反応物PhenylacetaldehydeHCID 998—
反応物Potassium CarbonateHCID 11430—
反応物Potassium hydroxy sulfiteHCID 23707502—
反応物5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoanilineHCID 67498806—
溶媒DimethylformamideHCID 6228—
生成物5-(Benzoxazol-2-yl)-2-benzyl-1-(tetrahydropyran-4-yl)benzimidazoleHCID 6749808042%

反応手順

To a solution of 5-(benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline (see Working Example 20-2) (200 mg, 0.646 mmol) in dimethylformamide (3 mL) was added phenylacetaldehyde (101 mg, 0.840 mmol) and oxone (258 mg, 0.420 mmol), and this was stirred at room temperature for 3 hours. After the reaction was complete, aqueous potassium carbonate solution was added, this was filtered and washed with water. The crystals obtained were purified by silica gel column chromatography to yield the title compound (110 mg, 42% yield) as light brown amorphous mass.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829035B2
出典データセットuspto-grants-2014_09
ORD IDord-0bbbe93463ce44a8911d4cac7a6abf1f
出典メモuspto-grants-2014_09