HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407966Generated: October 30, 2026
Potassium Carbonate → (S)-tert-butyl 4-(3-(1H-indazol-5-yloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate
https://huagongshe.com/reaction/407966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1H-Indazol-5-ol | HCID 101438 | — |
| Reactant | (R)-tert-butyl 4-(3-(methylsulfonyloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate | HCID 86688072 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (S)-tert-butyl 4-(3-(1H-indazol-5-yloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate | HCID 67470553 | 90% |
Reaction Steps
A flask was charged with 1H-indazol-5-ol (0.89 g, 0.66 mmol), (R)-tert-butyl 4-(3-(methylsulfonyloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (Preparation D; 0.2 g, 0.55 mmol), K2CO3 (0.092 g, 0.66 mmol), and DMSO (4 mL). The reaction was stirred at 130° C. overnight. Added water and extracted with ethyl acetate. The organic layers were combined, dried, filtered and concentrated. The residue was purified using silica gel column chromatography with 50-100% ethyl acetate in hexanes to provide (S)-tert-butyl 4-(3-(1H-indazol-5-yloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (0.198 g, 90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08754226B2 |
|---|
| Source dataset | uspto-grants-2014_06 |
|---|
| ORD ID | ord-7b415ac2b78c4b6b87f6a9cd7b4f4638 |
|---|
| Source note | uspto-grants-2014_06 |
|---|