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HRID 967855作成日:2026年10月27日

3-Chlorobenzenesulfonamide → 3-chloro-N-[({2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethyl}amino)carbonyl]benzenesulfonamide

https://huagongshe.com/reaction/967855

反応式

関与物質

役割名称HCID仕込み量
反応物3-ChlorobenzenesulfonamideHCID 519377—
反応物2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethylcarbamateHCID 22291350—
生成物3-chloro-N-[({2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethyl}amino)carbonyl]benzenesulfonamideHCID 22291347—

反応手順

The title compound was prepared according to the procedure described in step 2 of Example 18 from 2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethylcarbamate and 3-chlorobenzenesulfonamide. MS (ESI) m/z 509 [M+H]+, 507 [M−H]−, 1H-NMR (CDCl3)δ1.22 (3H, t, J=7.5 Hz), 2.68 (2H, q, J=7.5 Hz), 2.86 (2H, t, J=6.6 Hz), 3.47-3.56 (2H, m), 6.44 (1H, br), 7.23-7.28 (5H, m), 7.36 (2H, t, J=7.3 Hz), 7.45 (2H, t, J=8.1 Hz), 7.58 (2H, d, J=8.1 Hz), 7.73-7.78 (2H, m), 7.87 (1H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06956050B2
出典データセットuspto-grants-2005_10
ORD IDord-14353fad7dfb40f58fc27b4e76852a65
出典メモuspto-grants-2005_10