Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043679Generated: October 31, 2026

4-Propylpyrrolidin-2-one → HCID 53629223, compound

https://huagongshe.com/reaction/2043679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Propylpyrrolidin-2-oneHCID 14178100—
ReactantHCID 57743065HCID 57743065—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53629223HCID 5362922320%

Reaction Conditions

Temperature-30 °C

Reaction Steps

4-propylpyrrolidin-2-one x1 (0.22 g, 1.1 eq with respect to x199, 1.7 mmol) is dissolved in absolute THF (10 ml). A 1.06 M solution of Li—HMDS in THF (1.76 ml, 1.1 eq, 1.87 mmol) is added at −78° C. in a flow of argon. The reaction mixture is stirred for 15 min at −30° C. and cooled again to −78° C. A solution of 7-(chloromethyl)-3-(4-methoxybenzyl)-5-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine x202 in absolute THF (10 ml) is added dropwise at this temperature. The reaction mixture is allowed to heat up slowly to room temperature. In order to complete the reaction, the reaction mixture is refluxed the next morning for 1 h, and then partitioned between saturated aqueous NH4Cl and ethyl acetate. The organic layer is dried with anhydrous sodium sulfate and evaporated. The product is purified by HPLC (water/acetonitrile) to afford 0.14 g of 1-{[3-(4-methoxybenzyl)-5-(trifluoromethyl)-3H-imidazo[4,5-b]pyridin-7-yl]methyl}-4-propylpyrrolidin-2-one x205 (0.14 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586623B2
Source datasetuspto-grants-2013_11
ORD IDord-c3625db05dc640a09aa6d1b3c736b8a7
Source noteuspto-grants-2013_11