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HRID 1897475作成日:2026年10月26日

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

https://huagongshe.com/reaction/1897475

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物tert-Butyl 2-(bromomethyl)morpholine-4-carboxylateHCID 57418765—
反応物5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazol-6-olHCID 136163662—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylacetamideHCID 31374—
生成物5-(2,4-Difluorophenoxy)-1-isobutyl-6-(morpholin-2-ylmethoxy)-1H-indazoleHCID 67410279—

反応手順

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)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08518983B2
出典データセットuspto-grants-2013_08
ORD IDord-55f5e03fece24384963eb9db92cf3728
出典メモuspto-grants-2013_08