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HRID 594897作成日:2026年10月26日

Cesium carbonate → 6'-(3-Chloropyridin-2-yl)aminodispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetane]-2-amine

https://huagongshe.com/reaction/594897

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-Amino-3-chloropyridineHCID 693267—
反応物Di-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
反応物Di-tert-butyl (6'-bromodispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetan]-2-yl)imidodicarbonateHCID 86724239—
触媒(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one palladiumHCID 15673654—
溶媒1,4-DioxaneHCID 31275—
生成物6'-(3-Chloropyridin-2-yl)aminodispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetane]-2-amineHCID 8672429826.3%

反応条件

温度100 °C

反応手順

The mixture of di-tert-butyl (6′-bromodispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetan]-2-yl)imidodicarbonate (150 mg, 0.286 mmol), 3-chloropyridin-2-amine (184 mg, 1.43 mmol), (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one-palladium (3:2) (52 mg, 0.057 mmol), di-tert-butyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (97 mg, 0.23 mmol), and Cs2CO3(279 mg, 0.857 mmol) in 1,4-dioxane (7.5 ml) was stirred for 48 hours at 100° C. The reaction mixture was cooled down to ambient temperature, and partitioned with CHCl3 and water. The organic layer was dried over Na2SO4, and filtered. The residue was dissolved in toluene, and was added silica gel (neutral), and stirred at 130° C. for 3 hours. The mixture was concentrated under reduced pressure, and purified by silica gel column chromatography (CHCl3/MeOH=100:0-85:15) to give an amorphous, which was washed with CHCl3/hexane to give 6′-(3-chloropyridin-2-yl)aminodispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetane]-2-amine (28 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242973B2
出典データセットuspto-grants-2016_01
ORD IDord-74e4cc55ff924317b0f8348615ee7db3
出典メモuspto-grants-2016_01