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HRID 1896417作成日:2026年10月25日

Thionyl Chloride → 1-[(6-Methyl-2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)methyl]-4-propylpyrrolidin-2-one

https://huagongshe.com/reaction/1896417

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物1-(Hydroxymethyl)-4-propylpyrrolidin-2-oneHCID 11332602—
反応物6-Methyl-2-phenylpyrazolo[1,5-a]pyrimidineHCID 57743057—
溶媒TolueneHCID 1140—
生成物1-[(6-Methyl-2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)methyl]-4-propylpyrrolidin-2-oneHCID 5362912750%

反応条件

温度80 °C

反応手順

To a solution of 1-(hydroxymethyl)-4-propylpyrrolidin-2-one x2 (3.18 mmol, 1 eq, 0.5 g) in toluene (20 ml) is added thionyl chloride (3.5 mmol, 1.1 eq, 0.416 g). The mixture is stirred vigorously overnight at 80° C. After this time, 6-methyl-2-phenylpyrazolo[1,5-a]pyrimidine x122 (3.18 mmol, 1 eq, 0.665 g) and AlCl3 (3.18 mmol, 1 eq, 0.424 g) are successively added. The mixture is stirred at 80° C. for 2 hours. After evaporation of the solvent under reduced pressure, the crude mixture is poured to water and extracted with dichloromethane. The cumulated organic layers are dried over MgSO4, filtered over celite and evaporated under reduced pressure. The crude reaction mixture is purified by chromatography on silicagel (CH2Cl2/MeOH/NH4OH 98/2/0.2 (v/v/v)) and crystallized with AcOEt to afford 0.5 g of 1-[(6-methyl-2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)methyl]-4-propylpyrrolidin-2-one 202.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08518943B2
出典データセットuspto-grants-2013_08
ORD IDord-114a0710b86e40b8b913e682471cc5fa
出典メモuspto-grants-2013_08