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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1946499생성일: 2026년 10월 27일

Trimethylphosphine → Triethyl {3-[(4-chlorophenyl)methyl]-2-cyclopropyl-3,4,5,6-tetrahydrocyclopenta[d]imidazol-4-yl}methanetricarboxylate

https://huagongshe.com/reaction/1946499

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylphosphineHCID 68983—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물Triethyl methanetricarboxylateHCID 80471—
반응물3-[(4-Chlorophenyl)methyl]-2-cyclopropyl-3,4,5,6-tetrahydrocyclopenta[d]imidazol-4-olHCID 58460201—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물Triethyl {3-[(4-chlorophenyl)methyl]-2-cyclopropyl-3,4,5,6-tetrahydrocyclopenta[d]imidazol-4-yl}methanetricarboxylateHCID 58460194—

반응 조건

온도-78 °C

반응 단계

To a solution of Intermediate 30 (95 mg) and triethylmethanetricarboxylate (0.140 ml) in toluene (1.5 ml) and tetrahydrofuran (1.5 ml), stirred at RT under an inert atmosphere of nitrogen, was added trimethylphosphine, 1M in toluene (0.658 ml). The resulting solution was cooled to −78° C. and diisopropyl azodicarboxylate (0.130 ml) was added dropwise via syringe and the reaction was stirred at −78° C. for 45 mins. The reaction mixture was removed from the cold bath and allowed to warm to RT and stirred under N2 atmosphere overnight. Reaction mixture concentrated in vacuo. The residue was taken up in DCM (20 ml) and washed with water (20 mL). The 2 phases were separated, the organic extract was dried (hydrophobic frit) and concentrated under vacuum. The residue was purified on silica using a cyclohexane:ethyl acetate 0-100% gradient. The desired fractions were combined and concentrated under vacuum to give the title compound (146 mg). LC/MS MH+503, Rt 3.37 min (5 minute run).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399444B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-059c371ffae94ed4b77ca596bcd02ca7
출처 메모uspto-grants-2013_03