戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1617285作成日:2026年10月27日

Triethylamine → S-3304

https://huagongshe.com/reaction/1617285

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物p-EthynyltolueneHCID 13018—
反応物(R)-2-(5-Bromo-thiophene-2-sulfonylamino)-3-(1H-indol-3-yl)-propionic acidHCID 11396269—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物S-3304HCID 1071895655.4%

反応条件

温度50 °C

反応手順

In a round bottom flask was added crude (R)-2-(5-Bromo-thiophene-2-sulfonylamino)-3-(1H-indol-3-yl)-propionic acid (3) (60 mg, 0.14 mmol), p-tolyl acetylene 4 (480 mg, 0.41 mmol), PdCl2P(PPh3)2 (10 mg, 0.015 mmol), copper(I)iodide (2 mg, 0.01 mmol) and triethylamine (0.025 g, 0.25 mmol) and then dissolved in dry DMF (2 mL) under an atmosphere of nitrogen. The reaction mixture was then heated at 50° C. under a nitrogen atmosphere for 2 hours. The reaction mixture was then cooled to room temperature and diluted with ethyl acetate and washed with a solution composed of NaCl/NaHCO3/(NH4)2CO3/water (1:1:1:1) (×3), water, and then dried over sodium sulfate (Na2SO4). The crude product was purified using a SAX column to provide to give the desired (R)-3-(1H-Indol-3-yl)-2-(5-p-tolylethynyl-thiophene-2-sulfonylamino)-propionic acid 5 (0.036 g, 55%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08765953B2
出典データセットuspto-grants-2014_07
ORD IDord-2b120fd0b58f4976bcf5c3117d058314
出典メモuspto-grants-2014_07