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HRID 17886作成日:2026年10月26日

Triphenylphosphine → 6-(2-morpholine-4-yl ethoxy)-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amide

https://huagongshe.com/reaction/17886

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物2-MorpholinoethanolHCID 61163—
反応物Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
反応物HCID 178458041HCID 178458041—
溶媒BenzeneHCID 241—
溶媒TetrahydrofuranHCID 8028—
生成物6-(2-morpholine-4-yl ethoxy)-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amideHCID 8661402999%

反応手順

6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amide (7.0 g, 22.78 mmol) was dissolved in tetrahydrofuran:benzene (150 ml:50 ml). Then, hydroxyethylmorpholine (3.59 g, 27.33 mmol) and triphenyl phosphine (7.17 g, 27.33 mmol) were added thereto. When the temperature was adjusted to 0° C., diisopropyl azodicarboxylate (5.53 g, 27.33 mmol) was added dropwise to the mixture followed by stirring for 2 hours at room temperature. The mixture was washed with brine and extracted with ethyl acetate. The separated organic layer was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography to obtain 6-(2-morpholine-4-yl ethoxy)-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amide (9.5 g, yield 99%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741323B2
出典データセットuspto-grants-2010_06
ORD IDord-5da6139b69b8451d84463995d522f076
出典メモuspto-grants-2010_06