HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046502Generated: November 1, 2026
Acetonitrile → 1-Morpholino(4-(4-(tetrahydro-2H-pyran-4-yloxy)-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-yl)phenyl)methanone
https://huagongshe.com/reaction/1046502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | [4-(Morpholine-4-carbonyl)phenyl]boronic acid | HCID 2773546 | — |
| Reactant | HCID 66826813 | HCID 66826813 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Morpholino(4-(4-(tetrahydro-2H-pyran-4-yloxy)-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-yl)phenyl)methanone | HCID 66828967 | — |
Reaction Steps
3-iodo-4-(tetrahydro-2H-pyran-4-yloxy)-1-trityl-1H-pyrazolo[4,3-c]pyridine (100 mg, 0.170 mmol), 4-(morpholine-4-carbonyl)phenylboronic acid (48 mg, 0.204 mmol), and 1,1′-bis(diphenylphosphino)ferrocenepalladium chloride (13.9 mg, 0.017 mmol) were charged in a microwave vial equipped with a stir bar. Acetonitrile (1.0 mL) and 1.0 M potassium acetate in water (0.41 mL) were then added, the reaction mixture was degassed with nitrogen for 5 min and then heated to 150° C. under microwave irradiation for 40 min. The crude mixture was filtered through Celite®, and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08569281B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-6210529ed0b3448ab6cc90d77be35921 |
|---|
| Source note | uspto-grants-2013_10 |
|---|