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HRID 555888作成日:2026年10月25日

Cesium carbonate → tert-butyl 4-(3-(4-(1H-benzo[d]imidazole-2-carbonyl)phenoxy)pyrazin-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/555888

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N-methyl-2-pyrrolidoneHCID 13387—
反応物(1H-benzo[d]imidazol-2-yl)(4-hydroxyphenyl)methanoneHCID 59326874—
反応物Tert-butyl 4-(3-fluoropyrazin-2-yl)piperidine-1-carboxylateHCID 59351396—
溶媒WaterHCID 962—
生成物tert-butyl 4-(3-(4-(1H-benzo[d]imidazole-2-carbonyl)phenoxy)pyrazin-2-yl)piperidine-1-carboxylateHCID 59351389—

反応条件

温度150 °C

反応手順

To a 350 mL pressure vial is added tert-butyl 4-(3-fluoropyrazin-2-yl)piperidine-1-carboxylate (200 mg, 0.711 mmol), Cs2CO3 (417 mg, 1.280 mmol), and (1H-benzo[d]imidazol-2-yl)(4-hydroxyphenyl)methanone (305 mg, 1.280 mmol) and N-methylpyrrolidinone (1.3 mL). The reaction was heated in the microwave at 150° C. 1 h. The reaction was added to a flask containing H2O (20 mL) with rapid stirring. The resulting slurry was filtered and the solid filter cake washed with H2O (3×5 mL). The solid was purified by ISCO (40 g SiO2, 0-20% MeOH/CH2Cl2) to give tert-butyl 4-(3-(4-(1H-benzo[d]imidazole-2-carbonyl)phenoxy)pyrazin-2-yl)piperidine-1-carboxylate as a brown solid.

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-63d04538b8494a1c85be4e72e2a79890
出典メモuspto-grants-2011_11