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HRID 555801作成日:2026年10月25日

Potassium Carbonate → (4-(3-chloropyrazin-2-yloxy)phenyl)(1H-benzo[d]imidazol-2-yl)methanone

https://huagongshe.com/reaction/555801

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2,3-DichloropyrazineHCID 78575—
反応物HCID 21918119HCID 21918119—
反応物(1H-benzo[d]imidazol-2-yl)(4-hydroxyphenyl)methanoneHCID 59326874—
溶媒DimethylformamideHCID 6228—
生成物(4-(3-chloropyrazin-2-yloxy)phenyl)(1H-benzo[d]imidazol-2-yl)methanoneHCID 46207940—

反応条件

温度90 °C

反応手順

To a solution of compound (1H-benzo[d]imidazol-2-yl)(4-hydroxyphenyl)methanone (100 g, 0.42 mol) in anhydrous DMF (1.1 L) was added K2CO3 (145 g, 1.05 mol, 2.5 eq.) and 2,3-dichloropyrazine (75.08 g, 0.50 mol, 1.2 eq.). The reaction was stirred at 90° C. for 18 h. LCMS analysis of the reaction mixture showed that the reaction was complete. The reaction mixture was cooled to ambient temperature and ice-water (3 L) was added, stirred for 30 minutes. The resulting solid was filtered and washed with water (3 L) followed by MTBE (2×500 mL) and dried under vacuum. The solid was treated with 50% MTBE/DCM at 50° C. for 1 h and filtered hot, washed with 50% MTBE/DCM and dried under vacuum overnight to obtain product. Mother liquor was refluxed with 50% MTBE/DCM for 2 h and filtered hot and washed with 50% MTBE/DCM to get another batch of product. MS (ESI, pos. ion) m/z: 351.0 (M+1). IC50 (uM) +.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08053438B2
出典データセットuspto-grants-2011_11
ORD IDord-4f1aff02d9084fbda56f6331577ac737
出典メモuspto-grants-2011_11