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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1897475생성일: 2026년 10월 26일

Cesium carbonate → 5-(2,4-Difluorophenoxy)-1-isobutyl-6-(morpholin-2-ylmethoxy)-1H-indazole

https://huagongshe.com/reaction/1897475

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl 2-(bromomethyl)morpholine-4-carboxylateHCID 57418765—
반응물5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazol-6-olHCID 136163662—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DimethylacetamideHCID 31374—
생성물5-(2,4-Difluorophenoxy)-1-isobutyl-6-(morpholin-2-ylmethoxy)-1H-indazoleHCID 67410279—

반응 단계

To a solution of 5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazol-6-ol (0.035 g, 0.11 mmol) in DMA (3.5 mL) was added Cs2CO3 (0.11 g, 0.33 mmol). The mixture stirred at room temperature for 1 hour before the addition of 2-bromomethylmorpholine-4-carboxylic acid tert-butyl ester (0.062 g, 0.22 mmol). The resulting mixture was stirred at room temperature for 14 hours. The reaction mixture was diluted with ether and water and the layers were separated. The aqueous layer was extracted with ether (3×) and the combined organic layers were washed with water and brine, and dried over Na2SO4. The crude mixture was concentrated under reduced pressure and purified by reverse phase HPLC to afford the desired product. MS (APCI+) m/z 418 (M+1) detected; 1H NMR (400 mHz, CD3OD) δ 7.90 (s, 1H), 7.38 (s, 1H), 7.21 (s, 1H), 7.11 (m, 1H), 6.84 (m, 2H), 4.22 (m, 2H), 4.18 (d, 2H), 4.05 (m, 2H), 3.31 (m, 3H), 3.03 (m, 2H), 2.31 (m, 1H), 0.92 (d, 6H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08518983B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-55f5e03fece24384963eb9db92cf3728
출처 메모uspto-grants-2013_08