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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46873생성일: 2026년 10월 24일

Sodium Carbonate → 8-[3-(5-chloro-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/46873

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-oneHCID 70556—
반응물5-chloro-1,3-dihydro-2-oxo-2H-benzimidazole-1-propanol methanesulfonateHCID 21424816—
용매DimethylformamideHCID 6228—
생성물8-[3-(5-chloro-1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-oneHCID 2038558525%

반응 단계

A mixture of 4.9 parts of 5-chloro-1,3-dihydro-2-oxo-2H-benzimidazole-1-propanol methanesulfonate, 3.7 parts of 1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one, 3.4 parts of sodium carbonate and 90 parts of N,N-dimethylformamide is stirred and heated for 1 hour at 50°-60° C. The N,N-dimethylformamide is distilled off and the residue is taken up in water. The product is extracted with 4-methyl-2-pentanone. 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 residue solidifies on triturating in 4-methyl-2-pentanone. The product is filtered off and crystallized twice: first from 2-propanol and then from a mixture of N,N-dimethylformamide and water, yielding 1.8 parts (25%) of 8-[3-(5-chloro-1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one; mp. 233.7° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04175129
출처 데이터셋uspto-grants-1979_11
ORD IDord-e5008fe0aff94439bbeef0212360b3e3
출처 메모uspto-grants-1979_11