戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1819776作成日:2026年10月25日

Hydrochloric Acid → 2,4-Dichloro-N-[3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenyl]benzenesulfonamide

https://huagongshe.com/reaction/1819776

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物WaterHCID 962—
反応物Benzenesulfonyl chloride, 2,4-dichloro-HCID 204419—
反応物3,5-Dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamineHCID 22148776—
溶媒PyridineHCID 1049—
生成物2,4-Dichloro-N-[3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenyl]benzenesulfonamideHCID 1020958646.4%

反応手順

A solution of 3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamine (102) (2.0 g, 5.79 mmol) and 2,4-dichloro benzenesulfonylchloride (1.5 g, 6.08 mmol) in pyridine (10 mL) was stirred at room temperature for 12 h. Water was added to the reaction mixture, which was then acidified by 2N HCl. Reaction mixture was extracted twice with AcOEt. Organic layer was washed by brine, dried over MgSO4 and concentrated. Crude residue was purified by column chromatography (H/A=4/1, 80 g of silica gel) to afford title compound (104) (1.49 g, 46%) as a white solid. Mp 73-75° C. 1H NMR (300 MHz, DMSO-d6) δ 7.29 (2H, s), 7.46 (1H, dd, J=2.2, 8.8 Hz), 7.69 (1H, d, J=8.8 Hz), 7.71 (1H, dd, J=2.2, 8.4 Hz), 7.95 (1H, d, J=2.2 Hz), 8.14 (1H, d, J=2.2 Hz), 8.18 (1H, d, J=8.4 Hz), 11.5 (1H, br s). MS (M+H) 553.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07601841B2
出典データセットuspto-grants-2009_10
ORD IDord-aa67c3ec773d415bb3ff7f666cc90869
出典メモuspto-grants-2009_10