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HRID 277421作成日:2026年10月23日

Hydrochloric Acid → 3-(4-chloro-6-fluoro-3-methyl-2-nitrophenyl)-6-trifluoromethyl-2,4(1H, 3H)-pyrimidinedione

https://huagongshe.com/ja/reaction/277421

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-fluoro-5-methyl-6-nitro-N-phenoxycarbonylanilineHCID 18615646—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-(4-chloro-6-fluoro-3-methyl-2-nitrophenyl)-6-trifluoromethyl-2,4(1H, 3H)-pyrimidinedioneHCID 86585901104.9%

反応条件

温度-10 °C

反応手順

Ethyl 3-amino-4,4,4-trifluorocrotonate (6.1 g, 33.1 mmol) was dissolved in dimethylformamide (47 ml) and stirred at −10 ° C. To this solution was slowly added 1,8-diazabicyclo[5.4.0]undec-7-ene (6.3 g, 41.4 mmol) and solution stirred for 0.5 hr. To this solution was slowly added a solution of 4-chloro-2-fluoro-5-methyl-6-nitro-N-phenoxycarbonylaniline (8.5 g) in dimethylformamide (25 ml) followed by stirring at ambient temperature for 14 hr. Solution was then heated to 80 ° C. and stirred at this temperature for 4 hr. Water was added and pH adjusted to 4 by addition of dilute hydrochloric acid. Product was extracted with ethyl acetate followed by evaporation of the solvent to afford the crude product (10.1 g) which was subjected to N-methylation as follows.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355799B1
出典データセットuspto-grants-2002_03
ORD IDord-25819bacf4194d958d5590a297597818
出典メモuspto-grants-2002_03