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HRID 64436作成日:2026年10月25日

Sulfuric acid magnesium salt (1:1) → methyl (3S)-3-{[(1S)-1-(4-methoxyphenyl)ethyl]amino}indane-1-carboxylate

https://huagongshe.com/reaction/64436

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物(S)-1-(4-Methoxyphenyl)ethylamineHCID 793467—
反応物Methyl 3-oxo-2,3-dihydro-1H-indene-1-carboxylateHCID 2753058—
反応物Sodium borohydrideHCID 4311764—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
生成物methyl (3S)-3-{[(1S)-1-(4-methoxyphenyl)ethyl]amino}indane-1-carboxylateHCID 86713453—

反応手順

To a solution of 1 g of methyl 3-oxoindane-1-carboxylate in 10 ml of toluene were added 0.78 ml of (1S)-1-(4-methoxyphenyl)ethanamine and 100 mg of p-toluenesulfonic acid monohydrate, followed by heating to reflux for 5 hours using a Dean-Stark type reflux device. Then, 634 mg of magnesium sulfate was added thereto, followed by heating to reflux for 5 hours using a Dean-Stark type reflux device. Further, 634 mg of magnesium sulfate was added thereto, followed by heating to reflux for 5 hours using a Dean-Stark type reflux device. The insoluble material was removed by filtration and the solvent was then evaporated under reduced pressure to obtain an intermediate product. To a solution of the obtained intermediate product in 17 ml of ethanol was added 209 mg of sodium borohydride under ice-cooling, followed by stirring for 1 hour under ice-cooling. The solvent was evaporated under reduced pressure, and to the obtained residue were added water, a saturated aqueous sodium hydrogen carbonate solution, and ethyl acetate to carry out a layer separation operation. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 1.195 g of methyl (3S)-3-{[(1S)-1-(4-methoxyphenyl)ethyl]amino}indane-1-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447090B2
出典データセットuspto-grants-2016_09
ORD IDord-9349328707fc41c88b1215c50e613905
出典メモuspto-grants-2016_09