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HRID 1578393作成日:2026年10月27日

1-(p-Fluoro-phenyl)-4-[4-(2-oxo-1-benzimidazolinyl)-1,2,3,6-tetrahydro-1-pyridyl]-1-butanol → Droperidol

https://huagongshe.com/reaction/1578393

反応式

関与物質

役割名称HCID仕込み量
反応物1-(p-Fluoro-phenyl)-4-[4-(2-oxo-1-benzimidazolinyl)-1,2,3,6-tetrahydro-1-pyridyl]-1-butanolHCID 21559984—
触媒HCID 178418406HCID 178418406—
溶媒ChloroformHCID 6212—
生成物DroperidolHCID 3168—

反応手順

To a stirred solution of 2.0 g of 1-(p-fluoro-phenyl)-4-[4-(2-oxo-1-benzimidazolinyl)-1,2,3,6-tetrahydro-1-pyridyl]-1-butanol in 60 ml of chloroform at room temperature, was added portionwise 3.2 g of a fine powder of manganese dioxide. After completion of addition, the mixture was stirred for another 2 hours at room temperature, and the precipitate was filtered off. The filtrate was concentrated to dryness under reduced pressure, and the residue was recrystallized from dioxane containing water, to obtain γ-[4-(2-oxo-1-benzimidazolinyl)-1,2,3,6-tetrahydro-1-pyridyl]-p-fluorobutyrophenone, melting at 146° - 147 5°C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03936468
出典データセットuspto-grants-1976_02
ORD IDord-3bbf78a810714b19b60b7b5a6d10cd9a
出典メモuspto-grants-1976_02