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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2259989생성일: 2026년 10월 26일

Carbon Dioxide → N,N-Dimethyl-1H-imidazole-1-sulfonamide

https://huagongshe.com/reaction/2259989

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물TetralinHCID 8404—
반응물Ethyl chloroformateHCID 10928—
반응물N,N-Dimethyl 4-iodo-1H-imidazole-1-sulfonamideHCID 2773390—
반응물1,1,4,4,7-Pentamethyl-6-ethynyl-1,2,3,4-tetrahydronaphthaleneHCID 11806387—
반응물TrimethylaluminumHCID 16682925—
반응물ethyl (E)-4-[2-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethylnaphthalen-2-yl)propen-1-yl]-1-(N,N-dimethylsulfamoyl)-2-imidazolecarboxylateHCID 86749151—
반응물ButyllithiumHCID 178418339—
반응물HCID 178418361HCID 178418361—
반응물HCID 178470243HCID 178470243—
촉매Zirconocene dichiorideHCID 131716798—
촉매HCID 178418397HCID 178418397—
생성물N,N-Dimethyl-1H-imidazole-1-sulfonamideHCID 395751—

반응 단계

It should be noted in connection with Reaction Schemes 1, 2 and 3 that in all of these reaction schemes heterocycle derivatives corresponding respectively to Formula 7, 11 and 15 can be employed where in the A-B' substituent A is (CH2)n, n is 0, and B' is hydrogen. A carboxylic acid group is then introduced into the molecule, after coupling with the tetrahydronaphthalene moiety, by reaction with strong base (such as n-butyl lithium) and carbon dioxide or ethyl chloroformate. Reaction Scheme 4 illustrates specifically the synthesis of Compound 3 and Compound 4 of the present application. In accordance with this scheme (5,6,7,8-tetrahydro-3,5,5,8,8-pentamethylnaphthalen-2-yl)acetylene (Compound 10) is reacted with trimethylaluminum in the presence zirconocene dichloride. The resulting "carboaluminated adduct" (not shown in Scheme 4) is reacted in the presence of tetrakis(triphenylphosphine)palladium (Pd(PPh3)4) catalyst, with 1-(N,N-dimethylsulfamoyl)-4-iodoimidazole (Compound 11) which is obtained by iodination from 1-(N,N-dimethylsulfamoyl)imidazole. The latter compound can be obtained in accordance with the chemical literature: Chadwick et al. J. Chem. Soc., Perkin Trans. I 1984, 481-486. The result of the coupling reaction between between the carboaluminated adduct derived from Compound 10 and Compound 11 is (E)-4-[2-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethylnaphthalen-2-yl)propen-1-yl]-1-(N,N-dimethylsulfamoyl)imidazole (Compound 12). The carboxylic acid ethyl ester moiety is introduced into the molecule by reacting the anion of Compound 12 generated with strong base such as n-butyl lithium, with ethyl chloroformate, to yield ethyl (E)-4-[2-(5,6,7,8-tetrahydro- 3,5,5,8,8-pentamethylnaphthalen-2-yl)propen-1-yl]-1-(N,N-dimethylsulfamoyl)-2-imidazolecarboxylate (Compound 4). The dimethylsulfamoyl group is removed from the imidazole nitrogen by treatment with acid, to yield ethyl (E)-4-[2-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethylnaphthalen-2-yl)propen-1-yl]-2-imidazolecarboxylate (Compound 3). ##STR10##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05475113
출처 데이터셋uspto-grants-1995_12
ORD IDord-ea12ca04a80d41878492628784e50f66
출처 메모uspto-grants-1995_12