戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2259989作成日:2026年10月27日

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

https://huagongshe.com/reaction/2259989

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物TetralinHCID 8404—
反応物Ethyl chloroformateHCID 10928—
反応物N,N-Dimethyl 4-iodo-1H-imidazole-1-sulfonamideHCID 2773390—
反応物1,1,4,4,7-Pentamethyl-6-ethynyl-1,2,3,4-tetrahydronaphthaleneHCID 11806387—
反応物TrimethylaluminumHCID 16682925—
反応物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-imidazolecarboxylateHCID 86749151—
反応物ButyllithiumHCID 178418339—
反応物HCID 178418361HCID 178418361—
反応物HCID 178470243HCID 178470243—
触媒Zirconocene dichiorideHCID 131716798—
触媒HCID 178418397HCID 178418397—
生成物N,N-Dimethyl-1H-imidazole-1-sulfonamideHCID 395751—

反応手順

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##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05475113
出典データセットuspto-grants-1995_12
ORD IDord-ea12ca04a80d41878492628784e50f66
出典メモuspto-grants-1995_12