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HRID 1913881作成日:2026年10月26日

Potassium Carbonate → 1-(1H-indol-5-yl)-6-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1913881

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(2R)-1-(3-chloropropyl)-2-methylpyrrolidineHCID 55301078—
反応物tert-butyl 5-[6-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}-2-oxo-3,4-dihydroquinolin-1(2H)-yl]-1H-indole-1-carboxylateHCID 66681975—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物1-(1H-indol-5-yl)-6-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}-3,4-dihydroquinolin-2(1H)-oneHCID 468661312.2%

反応条件

温度80 °C

反応手順

To a solution of tert-butyl 5-[6-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}-2-oxo-3,4-dihydroquinolin-1(2H)-yl]-1H-indole-1-carboxylate (Compound No. 41) prepared in the same manner as shown in Example 1 (0.050 g) in methanol (0.19 mL), water (0.3 mL) and potassium carbonate (0.041 g) were added and stirred at 80° C. for 2 hours. The reaction mixture was concentrated under reduced pressure, and the resulting residue was purified by NH-type preparative TLC (on three plates of 0.25 mm thickness, developing solvent: ethyl acetate) to give the titled compound (0.0090 g, 2.2%) as a colorless amorphous substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08609847B2
出典データセットuspto-grants-2013_12
ORD IDord-058d6b26b4484ba2a32b4e64a6bc7841
出典メモuspto-grants-2013_12