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HRID 30899作成日:2026年10月24日

Sulfurous Acid → N-(4-iodophenyl)-6-methyl-1,3-benzothiazol-2-amine

https://huagongshe.com/ja/reaction/30899

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfurous AcidHCID 1100—
反応物Ammonium HydroxideHCID 14923—
反応物BromineHCID 24408—
反応物N-(4-iodophenyl)-N'-(4-methylphenyl)thioureaHCID 5017958—
溶媒ChloroformHCID 6212—
生成物N-(4-iodophenyl)-6-methyl-1,3-benzothiazol-2-amineHCID 2198571997%

反応手順

A suspension of N-(4-iodophenyl)-N′-(4-methylphenyl)thiourea (0.62 g, 4.68 mmol) in chloroform (23 mL) was treated with a solution of bromine (2.65 g, 16.59 mmol) in chloroform (1 mL). The reaction mixture was stirred at rt for 5 minutes and then heated at 50° C. for 5 minutes. Then the reaction mixture was allowed to cool, and was treated with sulphurous acid until the orange color disappeared. The reaction mixture was neutralized by treatment with conc. ammonium hydroxide. More chloroform was then added to dissolve the precipitate. The layers was separated, and the organic layer was washed with water and brine, dried over sodium sulfate, filtered and concentrated to give N-(4-iodophenyl)-6-methyl-1,3-benzothiazol-2-amine (0.6 g, 97%). 1H NMR (400 MHz, DMSO-d6) δ 2.36 (s, 3H), 7.12 (m, 1H), 7.48 (d, 1H), 7.60 (m, 3H), 7.65 (m, 2H), 10.50 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423156B2
出典データセットuspto-grants-2008_09
ORD IDord-9043f7dd576c4a4bb0909f02be421dbe
出典メモuspto-grants-2008_09