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HRID 1475231作成日:2026年10月27日

Cesium carbonate → 5-(5-Methyl-1-{[3-(oxan-4-yloxy)phenyl]methyl}-1H-1,2,4-triazol-3-yl)-3-[4-(trifluoromethoxy)phenyl]-1,2,4-oxadiazole

https://huagongshe.com/reaction/1475231

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-BromotetrahydropyranHCID 13349654—
反応物HCID 86711921HCID 86711921—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物5-(5-Methyl-1-{[3-(oxan-4-yloxy)phenyl]methyl}-1H-1,2,4-triazol-3-yl)-3-[4-(trifluoromethoxy)phenyl]-1,2,4-oxadiazoleHCID 86711924—

反応条件

温度140 °C

反応手順

A mixture of Cs2CO3 (62.5 mg, 0.192 mmol), 3-((5-methyl-3-(3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazol-5-yl)-1H-1,2,4-triazol-1-yl)methyl)phenol (Example 59; 40.0 mg, 0.096 mmol) and 4-bromotetrahydro-2H-pyran (21.7 uL, 0.192 mmol) in DMF (0.48 mL) was heated at 140° C. for 1 h under microwave irradiation. The mixture was diluted with H2O and extracted with 4:1 CHCl3:i-PrOH. The organic layer was dried over MgSO4 and concentrated under reduced pressure; the residue was dissolved in DMSO and purified using Prep-HPLC to furnish the title compound; MS (ES+) C24H22F3N5O4 requires: 501. found 502 [M+H]+; 1H-NMR (600 MHz, CD3OD) δ ppm 8.29 (d, J=8.8 Hz, 2H), 7.35 (d, J=8.1 Hz, 2H), 7.28 (m, 1H), 6.89 (dd, J=8.1, 2.4 Hz, 1H), 6.80 (m, 2H), 5.41 (s, 2H), 4.47 (m, 1H), 3.95 (m, 2H), 3.57 (m, 2H), 2.54 (s, 3H), 2.01 (m, 2H), 1.75 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09018380B2
出典データセットuspto-grants-2015_04
ORD IDord-f86210d8bbdf4a1995f69e72ea31a855
出典メモuspto-grants-2015_04