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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29718생성일: 2026년 10월 26일

Triethylamine → Methyl 4-{2-[(benzofuran-2-yl-carbonyl)amino]ethylsulfanyl}benzoate

https://huagongshe.com/reaction/29718

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzofuran-2-carboxylic acidHCID 10331—
반응물Sodium BicarbonateHCID 516892—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물Methyl 4-(2-aminoethylsulfanyl)benzoate hydrochlorideHCID 66687893—
용매DimethylformamideHCID 6228—
생성물Methyl 4-{2-[(benzofuran-2-yl-carbonyl)amino]ethylsulfanyl}benzoateHCID 6668794638.8%

반응 단계

Methyl 4-(2-aminoethylsulfanyl)benzoate hydrochloride (0.248 g, 1.00 mmol), was combined with benzofuran-2-carboxylic acid (0.162 g, 1.00 mmol) and HBTU (0.379 g, 1.00 mmol) in DMF (5 ml) at room temperature. Triethylamine (0.307 ml, 2.2 mmol) was added and the reaction mixture was stirred at room temperature overnight. Saturated aqueous NaHCO3 (15 ml) was added to give precipitates which was broken up by the addition of water (20 ml). The solid was filtered and the cake was dissolved in ethyl acetate. The residual water was removed by pipette and hexane was added to give methyl 4-{2-[(benzofuran-2-yl-carbonyl)-amino]ethylsulfanyl}benzoate (0.138 g) as a gum which was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420089B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-14f61712884949cfaf2783c6c5b1ae07
출처 메모uspto-grants-2008_09