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HRID 19556作成日:2026年10月24日

Triphenylphosphine → 6-(2-morpholine-4-ylethoxy)-1-oxo-3-pheny-1H-indene-2-carboxylic acid cyclohexylamide

https://huagongshe.com/ja/reaction/19556

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6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamideHCID 68697166—
溶媒Tetrahydropyran benzeneHCID 86615313—
生成物6-(2-morpholine-4-ylethoxy)-1-oxo-3-pheny-1H-indene-2-carboxylic acid cyclohexylamideHCID 6869834988.3%

反応条件

温度0 °C

反応手順

6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamide (141 mg, 0.41 mmol) obtained in Step 3 was dissolved in tetrahydropyran/benzene (3 mL/2 mL), and 4-(2-hydroxyethyl)morpholine (99 μl, 0.82 mmol) and triphenylphosphine (215 mg, 0.82 mmol) were added thereto. Then, diisopropyl azodicarboxilate (149 μl, 0.82 mmol) was added slowly thereto at 0° C., and stirred for 2 hrs at RT. The resulting mixture washed with saturated saline and extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 165 mg of the titled compound (yield: 88.3%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745439B2
出典データセットuspto-grants-2010_06
ORD IDord-e8d480256d7b46968a7d67c25afe805a
出典メモuspto-grants-2010_06