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HRID 366314作成日:2026年10月26日

Hydrochloric Acid → 3-(4-Chloro-2-ethyl-6-fluorobenzofuran-7-yl)-6-trifluoromethyluracil

https://huagongshe.com/reaction/366314

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物Ethyl 3-amino-4,4,4-trifluorocrotonateHCID 5702529—
反応物4-Chloro-2-ethyl-6-fluoro-7-phenoxycarbonylaminobenzofuranHCID 23289180—
溶媒DimethylformamideHCID 6228—
生成物3-(4-Chloro-2-ethyl-6-fluorobenzofuran-7-yl)-6-trifluoromethyluracilHCID 2328917644%

反応条件

温度60 °C

反応手順

80 ml of N,N-dimethylformamide was added to 5.8 g (32 mmol) of ethyl 3-amino-4,4,4-trifluorocrotonate and 6.6 g (43 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene, and 9.6 g (29 mmol) of 4-chloro-2-ethyl-6-fluoro-7-phenoxycarbonylaminobenzofuran was gradually added thereto at room temperature. After stirring at 60° C. for 8 hours, the reaction solution was poured into a 10% hydrochloric acid aqueous solution and acidified, and then extracted with ethyl acetate. The organic layer was washed sequentially with water and a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. Then, the obtained residue was purified by silica gel column chromatography to obtain 4.8 g (yield: 44%) of the desired product as white crystals. Melting point: 154-155° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06130187
出典データセットuspto-grants-2000_10
ORD IDord-8111caab964842e98b7fbc19b9ef2c26
出典メモuspto-grants-2000_10