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HRID 1723493作成日:2026年10月26日

1,4-Dioxane → 1-Butyl-3-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-2,4-imidazolidinedione

https://huagongshe.com/reaction/1723493

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DioxaneHCID 31275—
反応物Phenyl N-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)carbamateHCID 981607—
反応物ethyl N-butylglycineHCID 22062329—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒WaterHCID 962—
生成物1-Butyl-3-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-2,4-imidazolidinedioneHCID 13732377—

反応手順

A mixture of 24 parts of phenyl [4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]carbamate, 15.9 parts of ethyl N-butylglycine, 2 parts of N,N-dimethyl-4-pyridinamine and 200 parts of 1,4-dioxane was stirred and refluxed overnight. Then water was added and stirring was continued for a while. The reaction mixture was cooled, poured onto water and the whole was stirred. The precipitated product was filtered off, washed with water and dissolved in 150 parts of trichloromethane. This solution was stirred for 30 minutes with 3 parts of silica gel. The latter was filtered off and the filtrate was evaporated. The residue was crystallized from butanol. The product was filtered off and dried in vacuo at 60° C., yielding 2.3 parts of 1-butyl-3-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-2,4-imidazolidinedione; mp. 183.7° C. (39).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04861879
出典データセットuspto-grants-1989_08
ORD IDord-f906d22b3ef146ccad416484d2da789c
出典メモuspto-grants-1989_08