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HRID 34910作成日:2026年10月26日

Triethylamine → 4-(3-Indolyl)-1-[(4-oxo-3-thiazolidinyl)acetyl]piperidine

https://huagongshe.com/reaction/34910

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-(4-Piperidinyl)-1H-indoleHCID 702235—
反応物4-Oxo-3-thiazolidinylacetyl chlorideHCID 21297225—
溶媒ChloroformHCID 6212—
溶媒TetrahydrofuranHCID 8028—
生成物4-(3-Indolyl)-1-[(4-oxo-3-thiazolidinyl)acetyl]piperidineHCID 2129722227.5%

反応手順

A solution of 4-oxo-3-thiazolidinylacetyl chloride (1.75 g) in tetrahydrofuran (5.00 ml) was added dropsise to a suspension of 3-(4-piperidyl)indole (2.00 g) and triethylamine (4.10 ml) in a mixture of tetrahydrofuran (15.0 ml) and chloroform (5.00 ml) at 4° to 7° C. with stirring. After the mixture was allowed to stir for 1 hour with ice-bath cooling, the resultant precipitate was removed by filtration and the solvent was evaporated in vacuo. The residue was mixed with saturated aqueous sodium hydrogen carbonate (10.0 ml) and the mixture was extracted with chloroform (20.0 ml). The extract was washed with water, dried over magnesium sulfate and evaporated in vacuo. The residue was recrystallized from a mixture of methanol and acetone to give 4-(3-indolyl)-1-[(4-oxo-3-thiazolidinyl)acetyl]piperidine (0.92 g) as slightly brown prisms.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04764514
出典データセットuspto-grants-1988_08
ORD IDord-0003897d204849bf86b2e0ba626abee7
出典メモuspto-grants-1988_08