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HRID 17897作成日:2026年10月25日

Hydrochloric Acid → 3-phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate cyclohexylamide

https://huagongshe.com/reaction/17897

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物CyclohexylamineHCID 7965—
反応物TriethylamineHCID 8471—
反応物Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
反応物3-Phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylateHCID 86614033—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物3-phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate cyclohexylamideHCID 8661403259.8%

反応手順

3-Phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate (200 mg, 0.52 mmol) was dissolved in dichloromethane (10 ml). Triethylamine (240 μl, 1.72 mmol) and cyclohexylamine (59 μl, 0.52 mmol) were added thereto at 10° C. Then, after adding bis(2-oxo-3-oxazolidinyl)phosphinic chloride (137 mg, 0.52 mmol), the reaction mixture was stirred for about 20 min at room temperature followed by additional 1 hour at 10° C. After the water was added thereto to complete the reaction, pH was adjusted to 1˜1.5 with 4N hydrochloric acid. The mixture was washed with brine, and extracted with dichloromethane. The extract was dried over anhydrous sulfonate sulfate, concentrated, and the resulting residue was purified by column chromatography (ethyl acetate:hexane=1:9˜2:8) to obtain the title compound (yield 59.8%) as a red solid.

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-b7a74c8b2c8249d2bb1e621f9135b741
出典メモuspto-grants-2010_06