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HRID 46876作成日:2026年10月24日

1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-one → 8-[3-(5,6-dichloro-1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one

https://huagongshe.com/ja/reaction/46876

反応式

関与物質

役割名称HCID仕込み量
反応物1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-oneHCID 70556—
反応物5,6-dichloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonateHCID 86735357—
溶媒DimethylformamideHCID 6228—
生成物8-[3-(5,6-dichloro-1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-oneHCID 20385635—

反応条件

温度60 °C

反応手順

A mixture of 8 parts of 5,6-dichloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate, 9.2 parts of 1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one and 90 parts of N,N-dimethylformamide is stirred and heated at 60° C. for one hour. The reaction mixture is evaporated and water is added to the residue. The whole is alkalized with ammonium hydroxide and the product is extracted with trichloromethane. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 10% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The solid residue is triturated in 4-methyl-2-pentanone. The product is filtered off and dried, yielding 2 parts of 8-[3-(5,6-dichloro-1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one; mp. 275.2° 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-cce1ca1e5a0d4ef08faa92ec82b6e038
出典メモuspto-grants-1979_11