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HRID 710068作成日:2026年10月26日

Cesium carbonate → (S)-2,2-Difluoro-2-(1-hydroxy-3,3,5,5-tetramethylcyclohexyl)-1-(2-(5-((pyridazin-4-yloxy)methyl)isoxazol-3-yl)pyrrolidin-1-yl)ethanone

https://huagongshe.com/reaction/710068

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(1,1'-Binaphthalen)-2-yldi-tert-butylphosphineHCID 2734941—
反応物4-Bromopyridazine hydrobromideHCID 53407906—
反応物(S)-2,2-Difluoro-2-(1-hydroxy-3,3,5,5-tetramethylcyclohexyl)-1-(2-(5-(hydroxymethyl)isoxazol-3-yl)pyrrolidin-1-yl)ethanoneHCID 86706747—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
生成物(S)-2,2-Difluoro-2-(1-hydroxy-3,3,5,5-tetramethylcyclohexyl)-1-(2-(5-((pyridazin-4-yloxy)methyl)isoxazol-3-yl)pyrrolidin-1-yl)ethanoneHCID 8670678116.7%

反応条件

温度100 °C

反応手順

A sealed tube was charged with a mixture prepared by adding toluene (2 ml) to Compound 18 (30 mg), 4-bromopyridazine hydrobromide (22 mg), Pd(OAc)2 (2 mg), Cs2CO3 (37 mg), and [1,1′-binaphthalen]-2-yldi-tert-butylphosphine (3 mg) and the mixture was stirred at 100° C. for 4 hours. After cooling the reaction mixture to room temperature, NH silica gel was added, followed by stirring for a while. After separating the silica gel by filtration, the silica gel was washed with chloroform and the solvent was distilled off; the resulting residue was purified by reverse-phase preparative HPLC to give the titled compound (6.0 mg, colorless oil.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181229B2
出典データセットuspto-grants-2015_11
ORD IDord-a77022a34471403ea39f5d751aafaa39
出典メモuspto-grants-2015_11