HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028958Generated: October 25, 2026
Potassium Phosphate, Tribasic → 2-(2-Amino-3-morpholinoquinolin-6-yl)-3-methylbenzonitrile
https://huagongshe.com/reaction/1028958
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 2-Bromo-3-methylbenzonitrile | HCID 15469115 | — |
| Reactant | 3-Morpholino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amine | HCID 67347995 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(2-Amino-3-morpholinoquinolin-6-yl)-3-methylbenzonitrile | HCID 67345055 | — |
Reaction Steps
To a mixture of potassium phosphate (5.98 g, 28.2 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (0.54 g, 1.13 mmol), Pd2(dba)3 (0.26 g, 0.28 mmol), 2-bromo-3-methylbenzonitrile (2.21 g, 11.26 mmol) and 3-morpholino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amine (2.00 g, 5.63 mmol, prepared as in Example 2, Step 1-2) was added dioxane (50.0 mL) and water (25.0 mL). The mixture was heated to 140° C. for 10 min. The reaction mixture was allowed to cool to RT, filtered and then partitioned between EtOAc and water. The organic layer was washed with water and brine, and concentrated. The residue was diluted with EtOAc and then filtered. The solid was dried in air to afford 2-(2-amino-3-morpholinoquinolin-6-yl)-3-methylbenzonitrile as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08735384B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-7f6f23c9a4ae497b955691427325cfcf |
|---|
| Source note | uspto-grants-2014_05 |
|---|