Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | HCID 59851096 | HCID 59851096 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 56946585 | HCID 56946585 | — |
Reaction Steps
To a solution of 2-amino-9-chloro-5H,7H-benzo[b]pyrimido[4,5-d]azepin-6-one (I-23) (148 mg, 0.568 mmol), 1-bromobenzene (0.072 mL, 0.681 mmol), Cs2CO3 (333 mg, 1.02 mmol), and BINAP (53 mg, 0.085 mmol) in 4 mL toluene was added Pd(OAc)2 (12.8 mg, 0.057 mmol), and the reaction was stirred at 100° C. for 12 h. The reaction mixture was then treated with H2O and extracted with CH2Cl2 (2×30 mL). The organic fractions were combined, filtered, dried over MgSO4 and concentrated in vacuo to give an orange oil which was purified by C-18 RP LC-MS chromatography to afford I-61 (0.9%): HRMS Calcd. for C18H13ClN4O: 337.0856, Found 337.0853.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07459448B2 |
|---|
| Source dataset | uspto-grants-2008_12 |
|---|
| ORD ID | ord-e0b9a1bfaea94e3e97c0fc840e5a37fb |
|---|
| Source note | uspto-grants-2008_12 |
|---|