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HRID 41279作成日:2026年10月23日

Iodoethane → 3-[4-Ethoxy-2,6-dimethoxyphenyl]-6-methoxy-N-propyl-N-(tetrahydro-2H-pyran-4-yl)pyrazolo[5,1-b][1,3]thiazole-7-amine

https://huagongshe.com/ja/reaction/41279

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Potassium CarbonateHCID 11430—
反応物Sodium hydrideHCID 24758—
反応物1-IodopropaneHCID 33643—
反応物Tetrahydro-4H-pyran-4-oneHCID 121599—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物Tert-butyl[3-(4-hydroxy-2,6-dimethoxyphenyl)-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl]carbamateHCID 44479005—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物3-[4-Ethoxy-2,6-dimethoxyphenyl]-6-methoxy-N-propyl-N-(tetrahydro-2H-pyran-4-yl)pyrazolo[5,1-b][1,3]thiazole-7-amineHCID 5822349859.6%

反応手順

To a DMF (2.97 ml) solution of tert-butyl[3-(4-hydroxy-2,6-dimethoxyphenyl)-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl]carbamate (150 mg, 0.356 mmol) were added potassium carbonate (78.7 mg, 0.570 mmol) and iodoethane (45.6 μl, 0.570 mmol), and the mixture was stirred at room temperature for 16 hours and 10 minutes. Water was added to the reaction mixture, and the mixture was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was dissolved in DMF (1.88 ml), and sodium hydride (50% oil dispersion: 20.8 mg, 0.434 mmol) and 1-iodopropane (42.3 μl, 0.434 mmol) were added thereto, and the mixture was stirred at room temperature for 20 minutes. Ice was added to the reaction mixture, and the reaction mixture was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was dissolved in a mixture of dichloromethane (4.69 ml) and trifluoroacetic acid (1.87 ml), and the reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in a mixture of tetrahydrofuran (11.7 ml) and acetic acid (1.17 ml), tetrahydro-4H-pyran-4-one (61.5 μl, 0.670 mmol) and sodium triacetoxyborohydride (142 mg, 0.670 mmol) were added, and the mixture was stirred at mom temperature for 11 hours and 30 minutes. The reaction mixture was concentrated under reduced pressure, a saturated aqueous solution of sodium hydrogencarbonate was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the residue was purified by medium pressure silica gel column chromatography (n-heptane/ethyl acetate: 10% then 50%) to obtain the title compound (101 mg, 0.212 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530504B2
出典データセットuspto-grants-2013_09
ORD IDord-1048f2a749d74a92aa57603f733934dd
出典メモuspto-grants-2013_09