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HRID 390715作成日:2026年10月24日

Cesium carbonate → HCID 178426236、化合物

https://huagongshe.com/ja/reaction/390715

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2-Bromo-5-methylthiopheneHCID 69831—
反応物5-Chloro-1,10-phenanthrolineHCID 77865—
反応物2,2-dimethyl-N-(5-methyl-1,3-thiazol-2-yl)propanamideHCID 17190929—
反応物Water ammonium hydroxideHCID 86589665—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物HCID 178426236HCID 178426236—

反応条件

温度120 °C

反応手順

In a 4 mL vial charged with a stir bar, 2,2-dimethyl-N-(5-methyl-1,3-thiazol-2-yl)propanamide (62 mg, 0.3 mmol, Example 87A) was added, followed by copper(I) trifluoromethanesulfonate benzene complex (31 mg, 0.06 mmol), 5-chloro-1,10-phenanthroline (26 mg, 0.12 mmol) and cesium carbonate (107 mg, 0.33 mmol). A loose cap with septum was placed on the vial and then the vial was placed under vacuum in a vacuum oven for 30 minutes. The mixture was purged with nitrogen gas a couple of times. Then 2-bromo-5-methylthiophene (58 mg, 0.33 mmol) dissolved in 1-methyl-2-pyrrolidinone (1.0 mL) was added to the solid mixture. The vial was capped and placed on a heater/stirrer and heated to 120° C. overnight. Then 1 mL of a solution of concentrated ammonium hydroxide/water (1:2) was added. The reaction was filtered and concentrated to dryness. The residue was purified by reverse phase HPLC (C8, gradient 10-100% acetonitrile/water/0.1% trifluoroacetic acid) to provide the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383657B2
出典データセットuspto-grants-2013_02
ORD IDord-7e47200319224a43ab67caee20c0c6b9
出典メモuspto-grants-2013_02