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HRID 131846作成日:2026年10月27日

2-Aminothiazole → 2-(3,5-Dimethylphenylsulfanyl)nitrobenzene

https://huagongshe.com/reaction/131846

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminothiazoleHCID 2155—
反応物1-Fluoro-2-nitrobenzeneHCID 73895—
反応物3,5-DimethylbenzenethiolHCID 117548—
反応物2-((3,5-Dimethylphenyl)thio)anilineHCID 66998967—
生成物N-[2-(3,5-Dimethylphenylsulfanyl)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973312674%
生成物2-(3,5-Dimethylphenylsulfanyl)nitrobenzeneHCID 6699901778%

反応手順

2-(3,5-Dimethylphenylsulfanyl)nitrobenzene (1.01 g, 78%) was prepared from 3,5-dimethylthiophenol (0.76 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(3,5-dimethylphenylsulfanyl)aniline (0.64 g, 72%) following the general procedure B. N-[2-(3,5-Dimethylphenylsulfanyl)phenyl]-N′-(thiazol-2-yl)urea (131 mg, 74%) was prepared from 2-(3,5-dimethylphenylsulfanyl)aniline (115 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384967B2
出典データセットuspto-grants-2008_06
ORD IDord-e41ede9e832c434b94b3d4104ebcbf1e
出典メモuspto-grants-2008_06