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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46876생성일: 2026년 10월 24일

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/ko/reaction/46876

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-oneHCID 70556—
반응물5,6-dichloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonateHCID 86735357—
용매DimethylformamideHCID 6228—
생성물8-[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—

반응 조건

온도60 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04175129
출처 데이터셋uspto-grants-1979_11
ORD IDord-cce1ca1e5a0d4ef08faa92ec82b6e038
출처 메모uspto-grants-1979_11