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HRID 467802作成日:2026年10月25日

Dichloromethane → Benzyl 4-(4-chloro-5-trifluoromethylpyrimidin-2-ylamino)-benzoate

https://huagongshe.com/reaction/467802

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物DiisopropylethylamineHCID 81531—
反応物Benzyl p-aminobenzoateHCID 98488—
反応物2,4-Dichloro-5-(trifluoromethyl)pyrimidineHCID 2782774—
溶媒DimethylacetamideHCID 31374—
生成物Benzyl 4-(4-chloro-5-trifluoromethylpyrimidin-2-ylamino)-benzoateHCID 58809948—

反応条件

温度60 °C

反応手順

10 g (44 mmol) benzyl 4-aminobenzoate are dissolved in 200 mL DMA, 8 mL Hünig base (0.97 eq) are added and 10.4 g (48.21 mmol) 2,4-dichloro-5-trifluoromethylpyrimidine, dissolved in 50 mL DMA, are added dropwise at RT to this solution. The reaction mixture is stirred at 60° C. overnight, then combined with 300 mL DCM and extracted with water (3 times 300 mL). The organic phase is dried and the solvent is eliminated in vacuo. The crude product is combined with 100 mL MeOH, digested and left to stand for 2 h. Then it is stirred for 10 min, the precipitate is filtered off and washed with MeOH. Finally the crude product is again suspended in MeOH, filtered off, washed with a little MeOH and dried in the vacuum dryer at 60° C. 8.5 g A-2a are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08623887B2
出典データセットuspto-grants-2014_01
ORD IDord-8a32d504900b462eb107f58c27390590
出典メモuspto-grants-2014_01