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HRID 379980作成日:2026年10月25日

Sodium Carbonate → HCID 20692737、化合物

https://huagongshe.com/reaction/379980

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物2-(3-bromophenyl)-N-methylacetamideHCID 18668529—
反応物(1S,2R)-4-[2-(tert-butyldimethylsilanyloxy)-1-methyl-4-pyridin-3-ylbutoxy]benzeneboronic acidHCID 54020751—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
生成物HCID 20692737HCID 2069273777%

反応手順

A solution of (1S,2R)-4-[2-(tert-butyldimethylsilanyloxy)-1-methyl-4-pyridin-3-ylbutoxy]benzeneboronic acid (0.20 g, Example 11), 2-(3-bromophenyl)-N-methyl -acetamide (0.21 g, Example 12a)), 2M aqueous sodium carbonate (0.57 ml) and tetrakis(triphenylphosphine)palladium (0) (0.1 g) in toluene (5 ml) and ethanol (2 ml) was heated at 100° C. for 4 hours. After cooling, the solution was concentrated under reduced pressure. Concentrated hydrochloric acid (1 ml) was added to a solution of the residue in methanol (5 ml). The suspension was stirred at room temperature for 18 hours. The mixture was concentrated under reduced pressure and the residue partitioned between ether and water. The aqueous layer was neutralised and extracted with dichloromethane (2×50 ml). The combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by normal-phase HPLC eluting with a gradient of 0-25% ethanol in dichloromethane to give the title compound as an oil (0.15 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06300352B1
出典データセットuspto-grants-2001_10
ORD IDord-3598a98110e447a9b81a5785a84888de
出典メモuspto-grants-2001_10