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HRID 967825作成日:2026年10月25日

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

https://huagongshe.com/reaction/967825

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorobenzenesulfonamideHCID 66824—
反応物2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethylcarbamateHCID 22291350—
生成物4-chloro-N-[({2-[4-(2-ethyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethyl}amino)carbonyl]benzenesulfonamideHCID 10239272—

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 4-chlorobenzenesulfonamide. MS (ESI) m/z 509 [M+H]+, 507 [M−H]−, 1H-NMR (DMSO-d6) δ 1.14 (3H, t, J=7.5 Hz), 2.62 (2H, q, J=7.5 Hz), 2.72 (2H, t, J=7.1 Hz), 3.18-3.30 (2H, m), 6.60 (1H, t, J=5.7 Hz), 7.19 (1H, tt, J=7.3, 1.3 Hz), 7.28-7.38 (6H, m), 7.64-7.70 (2H, m), 7.76-7.80 (2H, m), 7.88 (2H, dt, J=11.2, 2.6 Hz).

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-bd6ea95aca4049e588eefbb023a216b3
出典メモuspto-grants-2005_10