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HRID 30906作成日:2026年10月24日

2-Amino-4-(trifluoromethyl)phenol → N-(4-Bromo-2-fluorophenyl)-5-(trifluoromethyl)-1,3-benzoxazol-2-amine

https://huagongshe.com/ja/reaction/30906

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4-(trifluoromethyl)phenolHCID 120246—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物4-Bromo-2-fluorophenylisothiocyanateHCID 2757003—
溶媒EthanolHCID 702—
生成物N-(4-Bromo-2-fluorophenyl)-5-(trifluoromethyl)-1,3-benzoxazol-2-amineHCID 2354934318%

反応手順

2-Amino-4-(trifluoromethyl)phenol (580 mg, 3.25 mmol) and 4-bromo-2-fluoro-1-isothio-cyanatobenzene (750 mg, 3.25 mmol) were stirred in ethyl alcohol at ambient temperature for 18 h. The flask was charged with 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (EDCI) (405 mg, 2.12 mmol), and the mixture was stirred for 2 h before being heated at reflux overnight. The reaction was allowed to cool to rt and was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and washed with 2 N aqueous hydrochloric acid solution and water, dried (Na2SO4), and concentrated in vacuo. The crude material was suspended in ether, sonicated, and the resulting solid was collected by filtration to provide the title compound (214 mg, 18%). LC-MS m/z 375.1 (MH+), retention time 3.70 minutes.

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-bbd0f4f801c04a91ae85780ff3f1de61
出典メモuspto-grants-2008_09