HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3-[1-(benzyloxy)-1H-pyrrolo[3,2-b]pyridin-6-yl]-N,N-dimethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Dimethylcarbamoyl)benzeneboronic acid | HCID 2773392 | — |
| Reactant | 1-(benzyloxy)-6-bromo-1H-pyrrolo[3,2-b]pyridine | HCID 67457727 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[1-(benzyloxy)-1H-pyrrolo[3,2-b]pyridin-6-yl]-N,N-dimethylbenzamide | HCID 46213945 | — |
Reaction Steps
A solution of 1-(benzyloxy)-6-bromo-1H-pyrrolo[3,2-b]pyridine (60 mg, 0.21 mmol, 1.0 eq), Pd(PPh3)4 (13 mg), 2.0 M K2CO3 (1.0 ml), DMF (1.2 ml), and [3-(dimethylcarbamoyl)phenyl]boronic acid (1.5 eq, 0.315 mmol) were reacted in microwave (110° C.) for 20 minutes. The upper layer was removed with a pipette and filtered, and purified with preparation HPLC to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912330B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-1c525d9490ac4ab2ad93348a13403001 |
| Source note | uspto-grants-2014_12 |