Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | HCID 59507478 | HCID 59507478 | — |
| Reactant | 5-Methoxyquinolin-3-amine | HCID 59507743 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59507926 | HCID 59507926 | — |
Reaction Steps
The desired compound was prepared as described in Example 2: Pd(OAc)2, BINAP, cesium carbonate, THF (0.8 mL) were mixed with 5-(6-chloro-2-morpholinopyrimidin-4-yl)pyrimidin-2-amine (1 eq.) and 5-methoxyquinolin-3-amine (2 eq), which was prepared as shown in Method 20. The mixture was heated under microwave irradiation for 10 minutes at 110° C. The solution was filtered and concentrated Under reduced pressure. The crude product was purified by preparative reverse phase HPLC. LC/MS (m/z): 431.2 (MH+), Rt 2.03 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563549B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-dfa34069afd946d2863c7c00b0ea2782 |
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| Source note | uspto-grants-2013_10 |
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