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HRID 46912作成日:2026年10月26日

Potassium Iodide → 1-{4-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]butyl}-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/46912

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Sodium CarbonateHCID 10340—
反応物4-(4-Chlorophenyl)-4-hydroxypiperidineHCID 38282—
反応物1-(4-chlorobutyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 13360889—
溶媒WaterHCID 962—
溶媒Methyl Isobutyl KetoneHCID 7909—
生成物1-{4-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]butyl}-1,3-dihydro-2H-benzimidazol-2-oneHCID 20385556—

反応手順

A mixture of 4.94 parts of 1-(4-chlorobutyl)-1,3-dihydro-2H-benzimidazol-2-one, 4.23 parts of 4-(4-chlorophenyl)-4-piperidinol, 5.3 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 20 hours with water-separator. The reaction mixture is cooled, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is crystallized from 4-methyl-2-pentanone. The product is filtered off and dried, yielding 4 parts of 1-{4-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]butyl}-1,3-dihydro-2H-benzimidazol-2-one; mp. 160.6° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04175129
出典データセットuspto-grants-1979_11
ORD IDord-f1478c099a5742d0be50314716473f92
出典メモuspto-grants-1979_11