HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038853Generated: October 25, 2026
Potassium Carbonate → HCID 67129987, compound
https://huagongshe.com/reaction/1038853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 7-amino-3-methyl-3,4-dihydroquinolin-2(1H)-one | HCID 15719033 | — |
| Reactant | 2-chloro-N-cyclopropylfuro[3,2-d]pyrimidin-4-amine | HCID 86665093 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67129987 | HCID 67129987 | 25.3% |
Reaction Steps
A flask was charged with 2-chloro-N-cyclopropylfuro[3,2-d]pyrimidin-4-amine (0.38 g, 1.8 mmol, Example #3, Step C), 7-amino-3-methyl-3,4-dihydroquinolin-2(1H)-one (0.30 g, 1.7 mmol), K2CO3 (0.38 g, 2.7 mmol), Pd2dba3 (0.17 g, 0.18 mmol) and X-Phos (0.17 g, 0.36 mmol) in 1,4-dioxane (20 mL). The flask was evacuated and purged with N2 (3×), and the mixture was heated to about 100° C. overnight. The mixture was cooled to rt and concentrated under reduced pressure to a residue. The residue was purified by preparative TLC (1.0 mm plate), eluting with DCM/MeOH (12:1). The product obtained was further purified by preparative HPLC (Table 2, Method r) to give 7-(4-(cyclopropylamino)furo[3,2-d]pyrimidin-2-ylamino)-3-methyl-3,4-dihydroquinolin-2(1H)-one (0.15 g, 24%): LC/MS (Table 2, Method g) Rt=1.04 min; MS m/z: 177 (M+H)+. Syk IC50=A
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08551981B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-93e5a8f7466f4f44a9ed2918ab0aaa13 |
|---|
| Source note | uspto-grants-2013_10 |
|---|