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HRID 967837作成日:2026年10月25日

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

https://huagongshe.com/reaction/967837

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phenyl 2-{4-[2-ethyl-4-(4-fluorophenyl)-1H-imidazol-1-yl]phenyl}ethylcarbamateHCID 22291420—
生成物4-chloro-N-{[(2-{4-[2-ethyl-4-(4-fluorophenyl)-1H-imidazol-1-yl]phenyl}ethyl)amino]carbonyl}benzenesulfonamideHCID 22291409—

反応手順

The title compound was prepared according to the procedure described in step 2 of Example 18 from phenyl 2-{4-[2-ethyl-4-(4-fluorophenyl)-1H-imidazol-1-yl]phenyl}ethylcarbamate and 4-chlorobenzenesulfonamide. MS (ESI) m/z 527 [M+H]+, 525 [M−H]−, 1H-NMR (CDCl3) δ 1.24 (3H, t, J=7.5 Hz), 2.69 (2H, q, J=7.5 Hz), 2.83-2.90 (2H, m), 3.45-3.54 (2H, m), 6.50 (1H, br), 7.05 (2H, t, J=8.8 Hz), 7.18 (1H, s), 7.22-7.30 (2H, m), 7.42-7.52 (3H, m), 7.70-7.79 (4H, 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-e25a5811901f428992744298d6ac8144
出典メモuspto-grants-2005_10