戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 891137作成日:2026年10月25日

3-Hydroxybenzenesulfonamide → 3-hydroxy-N-{[(2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethyl)amino]carbonyl}benzenesulfonamide

https://huagongshe.com/reaction/891137

反応式

関与物質

役割名称HCID仕込み量
反応物3-HydroxybenzenesulfonamideHCID 637557—
反応物Phenyl 2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethylcarbamateHCID 22244671—
生成物3-hydroxy-N-{[(2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethyl)amino]carbonyl}benzenesulfonamideHCID 22244698—

反応手順

The title compound was prepared according to the procedure described in step 1 of Example 42 from phenyl 2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethylcarbamate (step 7 of Example 52) and 3-hydroxybenzenesulfonamide: MS (ESI) m/z 545 [M+H]+, 543 [M−H]−, 1H-NMR (CDCl3) δ 7.48-7.01 (13H, m), 6.32 ▪ 1H, br.s), 3.50 (2H, t, J=6.1 Hz), 2.85 (2H, t, J=6.1 Hz), 2.20 (3H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07001917B2
出典データセットuspto-grants-2006_02
ORD IDord-e3e7291f2efb447ab7e0e6c4a8af5220
出典メモuspto-grants-2006_02