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HRID 530392作成日:2026年10月26日

Potassium Carbonate → Ethyl 3'-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}biphenyl-4-carboxylate

https://huagongshe.com/reaction/530392

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Ethyl 4-bromobenzoateHCID 22043—
反応物N-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-(trifluoromethyl)pyrimidin-2-amineHCID 58456307—
触媒HCID 178418807HCID 178418807—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 3'-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}biphenyl-4-carboxylateHCID 90041226—

反応条件

温度85 °C

反応手順

Ethyl 4-bromobenzoate (73.2 mg, 0.301 mmol) was added to a mixture of N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4-(trifluoromethyl)pyrimidin-2-amine (100 mg, 0.274 mmol), PdCl2(dppf)-CH2Cl2 adduct (22.4 mg, 0.027 mmol), DMF (5.5 mL), and aqueous K2CO3 (2 M, 0.411 mL, 0.822 mmol) and the reaction mixture was evacuated and back flushed with Argon. The reaction mixture was heated in the microwave reactor for 2 hours at 85° C. The reaction mixture was diluted with water, extracted with ethyl acetate, washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography (ethyl acetate/hexanes) to afford ethyl 3′-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}biphenyl-4-carboxylate as an off-white solid. MS ESI calc'd. for C20H17F3N3O2[M+H]+ 388, found 388. 1H NMR (500 MHz, CDCl3): δ 8.67 (d, J=4.9 Hz, 1H); 7.96 (s, 1H); 7.61 (t, J=6.2 Hz, 3H); 7.55 (s, 1H); 7.47-7.40 (m, 1H); 7.40 (d, J=7.9 Hz, 2H); 7.35 (d, J=7.7 Hz, 1H); 7.06 (d, J=4.9 Hz, 1H); 4.22 (q, J=7.1 Hz, 2H); 1.31 (t, J=7.1 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09353066B2
出典データセットuspto-grants-2016_05
ORD IDord-37c51c0918a34f29830c867fac9c1df1
出典メモuspto-grants-2016_05