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HRID 621201作成日:2026年10月27日

Hexane → N,N,5-Trimethyl-4-[(2,3,4,9-tetrahydro-9-methyl-4-oxo-1H-carbazol-3-yl) methyl]-1H-imidazole-1-sulphonamide

https://huagongshe.com/reaction/621201

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物TriethylamineHCID 8471—
反応物Dimethylsulphamoyl chlorideHCID 83372—
反応物GR 67330HCID 172316—
溶媒DichloromethaneHCID 6344—
生成物N,N,5-Trimethyl-4-[(2,3,4,9-tetrahydro-9-methyl-4-oxo-1H-carbazol-3-yl) methyl]-1H-imidazole-1-sulphonamideHCID 14233929—

反応手順

A solution of dimethylsulphamoyl chloride (0.16 ml) in dry dichloromethane was added to a stirred solution of 1,2,3,9-tetrahydro-9-methyl-3-[(5-methyl-1H-imidazol-4-yl)methyl]-4H-carbazol-4-one (438 mg) and triethylamine (0.25 ml) in dry dichloromethane (30 ml) and the mixture was heated at reflux for 18 h. After cooling the reaction mixture was adsorbed onto FCC silica which was then applied to a column and FCC eluting with System A (150:8:1) gave an oil, which solidified to a powder on trituration with dry hexane (30 ml). This powder was then further purified by dissolution in dry dichloromethane (30 ml) and crystallisation by addition of dry hexane (10 ml) to give the title compound (518 mg), m.p. 122°-124°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04822881
出典データセットuspto-grants-1989_04
ORD IDord-92df16e5fce8404c882045c4791a01ea
出典メモuspto-grants-1989_04