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HRID 1671665作成日:2026年10月26日

Ethyl Acetate → 3,4-Dimethoxy-N-(4-(3-nitrophenyl)-2-thiazolyl)benzenesulfonamide

https://huagongshe.com/reaction/1671665

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物2-Amino-4-(3-nitrophenyl)thiazoleHCID 613504—
反応物3,4-Dimethoxybenzenesulfonyl chlorideHCID 2734183—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
溶媒TolueneHCID 1140—
生成物3,4-Dimethoxy-N-(4-(3-nitrophenyl)-2-thiazolyl)benzenesulfonamideHCID 5282337—

反応手順

4-(3-Nitrophenyl)thiazol-2-amine (1.10 g, 5.0 mmol) was dissolved in dry pyridine (16 mL) and then 3,4-dimethoxybenzene-1-sulfonyl chloride (1.323 g, 5.59 mmol) was added. The reaction mixture was stirred at room temperature for 23 h and then the pyridine was flashed off in vacuo with toluene. The residue was slurried with EtOAc and water. Full solution was achieved and then ice cold 1M NaOH was added. After thorough shaking, the aqueous phase was separated and the organic phase was twice extracted with 1M NaOH and then with water until no yellow color was extracted. The aqueous extract was combined with the NaOH solution and the solution was made slightly acidic with 3M HCl. The product was extracted into EtOAc, then washed successively with H2O and saturated NaCl solution. After drying over Na2SO4, the solvent was removed in vacuo to give a gum which contained HOAc. This was flashed off with toluene. The foam remained slowly solidified and after drying in vacuo, weighed 1.632 g (77.4%) and was greater than 95% pure by TLC. This material was taken up in hot EtOAc, diluted with about one-half the volume of hexane while hot which induced crystallization. The first crop weighed 1.352 g and was pure by TLC, but had no distinct melting point. Yield of pure material (TLC) was 64.2%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07994338B2
出典データセットuspto-grants-2011_08
ORD IDord-185d2e1556024d5086d633133aec6910
出典メモuspto-grants-2011_08