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HRID 1971792作成日:2026年10月27日

Potassium Carbonate → tert-Butyl (3-{4-[(cyclobutyloxy)methyl]-2,6-dimethoxyphenyl}-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl)carbamate

https://huagongshe.com/reaction/1971792

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物TriphenylphosphineHCID 11776—
反応物(3-Bromo-6-methoxy-pyrazolo[5,1-b]thiazol-7-yl)-carbamic acid tert-butyl esterHCID 57912433—
反応物{4-[(Cyclobutyloxy)methyl]-2,6-dimethoxyphenyl}boronic acidHCID 57912446—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
溶媒Ethyl AcetateHCID 8857—
生成物tert-Butyl (3-{4-[(cyclobutyloxy)methyl]-2,6-dimethoxyphenyl}-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl)carbamateHCID 5791246489.4%

反応条件

温度90 °C

反応手順

To a mixture of tert-butyl (3-bromo-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl)carbamate (987 mg, 2.83 mmol), DME (80 mL) and water (28 mL) were added {4-[(cyclobutyloxy)methyl]-2,6-dimethoxyphenyl}boronic acid (904 mg, 3.4 mmol), potassium carbonate (785 mg, 5.68 mmol), triphenylphosphine (370 mg, 1.42 mmol) and palladium acetate (63.7 mg, 0.282 mmol) in that order, and the mixture was stirred at 90° C. (internal temperature) for 3 hours. Water was added to the reaction mixture, and then ethyl acetate was added. After thoroughly shaking the mixture, the organic layer was separated and the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The mixture was filtered, and then the solvent in the filtrate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (mixture of n-heptane and ethyl acetate: n-heptane/ethyl acetate=2/1) to obtain the title compound (1.24 g, 2.53 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08431603B2
出典データセットuspto-grants-2013_04
ORD IDord-c00b2c3d15a94d3cbcfc301c34f7af67
出典メモuspto-grants-2013_04