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HRID 629062作成日:2026年10月25日

3-Pyrimidin-5-yl-benzoic acid → 3-(Pyrimidin-5-yl)-N-(4-(2,2,2-trifluoroethyl)phenyl)benzamide

https://huagongshe.com/reaction/629062

反応式

関与物質

役割名称HCID仕込み量
反応物3-Pyrimidin-5-yl-benzoic acidHCID 4187250—
反応物4-(2,2,2-Trifluoroethyl)anilineHCID 14836858—
溶媒DichloromethaneHCID 6344—
生成物3-(Pyrimidin-5-yl)-N-(4-(2,2,2-trifluoroethyl)phenyl)benzamideHCID 72203011—

反応手順

A mixture of 3-pyrimidin-5-yl-benzoic acid (100 mg, 0.50 mmol) SOCl2 (73 μL, 1.0 mmol) was heated under reflux for 4 h. The solvent was evaporated off under reduced pressure and the residue was dissolved in DCM (5 mL) and slowly added to a mixture of 4-(2,2,2-trifluoroethyl)aniline (105 mg, 0.60 mmol) and TEA (140 μL, 1.0 mmol) in DCM (5 mL). The mixture was stirred at RT overnight. The solvent was evaporated off under reduced pressure and the residue was suspended in water (20 mL) filtered and dried under vacuum to afford the title compound. LC-MS (Condition 4) tR=1.05 min, m/z=375.8 [M+H]+; 1H-NMR (400 MHz, CDCl3) δ ppm 3.40 (q, J=10.76 Hz, 2H) 7.35 (d, J=8.56 Hz, 2H) 7.65-7.71 (m, 3H) 7.80 (d, J=7.82 Hz, 1H) 7.87-7.98 (m, 2H) 8.15 (s, 1H) 9.03 (s, 2H) 9.28 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09315489B2
出典データセットuspto-grants-2016_04
ORD IDord-558cfcfaa1894890bfcc2b5f9ea3663c
出典メモuspto-grants-2016_04