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HRID 1808166作成日:2026年10月25日

Water → 4-[(1,3-Thiazol-2-ylamino)sulfonyl]-N-(2-thienylmethyl)benzamide

https://huagongshe.com/reaction/1808166

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium CarbonateHCID 10340—
反応物Carbonate IonHCID 19660—
反応物(2-Thienylmethyl)amineHCID 34005—
反応物4-Iodo-N-(thiazol-2-yl)benzenesulfonamideHCID 1019318—
触媒palladium(II) acetateHCID 167845—
触媒HCID 178521658HCID 178521658—
溶媒Hydrochloric AcidHCID 313—
生成物4-[(1,3-Thiazol-2-ylamino)sulfonyl]-N-(2-thienylmethyl)benzamideHCID 57732211—

反応条件

温度110 °C

反応手順

4-Iodo-N-1,3-thiazol-2-ylbenzenesulfonamide Preparation 98, 200 mg, 0.5 mmol), thiophene-2-methanamine (280 uL, 2.7 mmol), hexacarbonylmolybdenum (70 mg, 0.3 mmol), palladium(II) acetate (6 mg, 0.03 mmol), and sodium carbonate (170 mg, 1.6 mmol) in water (1.1 mL, 61 mmol) was heated 30 min at 110° C. in the microwave. The reaction mixture was diluted with 1 N HCl and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was dissolved in methylene chloride/MeOH and MP-Carbonate (2.73 mmol/g loading; 1.0 g, 2.73 mmol) was added. After stirring 1 h, LC/MS analysis indicated complete capture of the target compound. The resin was washed with methylene chloride then stirred in 8:1 methylene chloride/AcOH. LC/MS analysis indicated the target compound was released from the resin (not quantified). The material was further purified on the Isco (12 g SiO2, ethyl acetate to 4:1 ethyl acetate-MeOH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08357711B2
出典データセットuspto-grants-2013_01
ORD IDord-c277c6b241404fae86005725c479e7c1
出典メモuspto-grants-2013_01