HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924319Generated: October 31, 2026
4-Propylpyrrolidin-2-one → HCID 53629223, compound
https://huagongshe.com/reaction/1924319
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Propylpyrrolidin-2-one | HCID 14178100 | — |
| Reactant | HCID 57743065 | HCID 57743065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53629223 | HCID 53629223 | 20% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08178533B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-a36bba85bb5e4b7cacb3fc1cc012393f |
|---|
| Source note | uspto-grants-2012_05 |
|---|