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HRID 354977作成日:2026年10月25日

Potassium Iodide → 1-[4-{4-[bis(4-fluorophenyl)methyl]-1-piperazinyl}butyl]-1,3-dihydro-2H-benzimidazol-2-one dihydrochloride

https://huagongshe.com/reaction/354977

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1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
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-[bis(4-fluorophenyl)methyl]-1-piperazinyl}butyl]-1,3-dihydro-2H-benzimidazol-2-one dihydrochlorideHCID 20506294—

反応手順

A mixture of 4.94 parts of 1-(4-chlorobutyl)-1,3-dihydro-2H-benzimidazol-2-one, 5.76 parts of 1-[bis(4-fluorophenyl)methyl]piperazine, 5.3 parts of sodium carbonate, 0.2 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 ethanol. The product is filtered off and dried, yielding 1-[4-{4-[bis(4-fluorophenyl)methyl]-1-piperazinyl}butyl]-1,3-dihydro-2H-benzimidazol-2-one dihydrochloride. hydrate; mp. 184.4° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04377578
出典データセットuspto-grants-1983_03
ORD IDord-93b7e8cf0b1043f6b1a856e75628d3a2
出典メモuspto-grants-1983_03