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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1160452생성일: 2026년 10월 27일

Dimethylformamide → 3-(2-Furyl)-5-[methyl(methylsulfonyl)amino]benzoic acid

https://huagongshe.com/reaction/1160452

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Lithium ChlorideHCID 433294—
반응물2-(Tributylstannyl)furanHCID 4393688—
반응물Methyl 3-bromo-5-[methyl(methylsulfonyl)amino]benzoateHCID 57529331—
용매Toluene ethylacetateHCID 21584019—
생성물3-(2-Furyl)-5-[methyl(methylsulfonyl)amino]benzoic acidHCID 5781511171%

반응 조건

온도100 °C

반응 단계

A mixture of methyl 3-bromo-5-[methyl(methylsulfonyl)amino]benzoate obtained in Reference Example 15 166 mg (0.5.0 mmol), tri-n-butyl(2-furyl)stannane 0.18 mL (0.55 mmol), lithium chloride 42 mg (0.10 mmol), tetrakistriphenylphosphine palladium(0) 29 mg (0.025 mmol) and N,N-dimethylformamide (1.5 mL) was stirred at 100° C. under argon atmosphere for 7 hours. The mixture was diluted with a mixed solvent of ethyl acetate/toluene=1:1 and washed twice with water. After drying of the mixture on magnesium sulfate, the mixture was concentrated and the residual oil was purified by a column chromatography on silica gel (eluted with hexane/ethyl acetate=2:1→1:1). The resulting solid was dissolved in a mixture of 2N aqueous sodium hydroxide solution (2 mL), methanol (2 mL) and tetrahydrofuran (2 mL) and the mixture was stirred at room temperature for 15 hours. The solvent was concentrated and thereto added water and the mixture was washed with a mixed solvent of hexane/ethyl acetate=1:1. The aqueous layer was adjusted by adding 1N hydrochloric acid to pH=3 and the mixture was extracted with ethyl acetate. After drying of the mixture on magnesium sulfate, the solvent was evaporated to give 105 mg (0.355 mmol) of the title compound (yield: 71%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07816387B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-3feca7309f124ea4be4a2cecc29e5aad
출처 메모uspto-grants-2010_10