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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1617285생성일: 2026년 10월 26일

Triethylamine → S-3304

https://huagongshe.com/reaction/1617285

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물p-EthynyltolueneHCID 13018—
반응물(R)-2-(5-Bromo-thiophene-2-sulfonylamino)-3-(1H-indol-3-yl)-propionic acidHCID 11396269—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물S-3304HCID 1071895655.4%

반응 조건

온도50 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08765953B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-2b120fd0b58f4976bcf5c3117d058314
출처 메모uspto-grants-2014_07