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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926791Generated: October 25, 2026

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

https://huagongshe.com/reaction/1926791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1-(Hydroxymethyl)-4-propylpyrrolidin-2-oneHCID 11332602—
Reactant6-Methyl-2-phenylpyrazolo[1,5-a]pyrimidineHCID 57743057—
SolventTolueneHCID 1140—
Product1-[(6-Methyl-2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)methyl]-4-propylpyrrolidin-2-oneHCID 5362912750%

Reaction Conditions

Temperature80 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183241B2
Source datasetuspto-grants-2012_05
ORD IDord-1eb99610806d4bf993576401d50f2313
Source noteuspto-grants-2012_05