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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13290생성일: 2026년 10월 24일

Cesium carbonate → Tert-butyl (3-fluoro-4-(6-methanesulfonyl-pyridin-3-yloxy)-phenyl)-carbamate

https://huagongshe.com/ko/reaction/13290

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물tert-Butyl (3-Fluoro-4-hydroxyphenyl)carbamateHCID 11708410—
반응물5-chloro-2-(methylsulfonyl)PyridineHCID 23145229—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl (3-fluoro-4-(6-methanesulfonyl-pyridin-3-yloxy)-phenyl)-carbamateHCID 86619205—

반응 조건

온도100 °C

반응 단계

4.00 g of 5-chloro-2-methanesulfonyl-pyridine and 8.80 g of cesium carbonate were added to an N-methylpyrrolidinone (50 ml) solution of 4.74 g of tert-butyl (3-fluoro-4-hydroxy-phenyl)-carbamate obtained in (step 1), and the reaction liquid was stirred at 100° C. for 2 hours. The reaction liquid was diluted with ethyl acetate, washed with water and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=1/1) to obtain the entitled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f25b9b9defd24663b180c955f8b5d0f7
출처 메모uspto-grants-2010_06