HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Phosphate, Tribasic → HCID 24825980, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Amino-4-methylthiazole | HCID 74143 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | Pyrimidine, 2-chloro-4-phenoxy- | HCID 12679944 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 24825980 | HCID 24825980 | 10.3% |
Reaction Steps
Using the method of Example 3, Step B, 4-methylthiazol-2-amine (7.66 mL, 3.07 mmol), 2-chloro-4-phenoxypyrimidine (0.697 g, 3.37 mmol), potassium phosphate (0.716 g, 3.37 mmol), Pd2(dba)3 (0.0702 g, 0.0766 mmol) and 4,5-bis(diphenylphosphino)-9,9-dimethyl-9H-xanthene (0.0488 g, 0.0843 mmol) were reacted in toluene (8 mL) and water (3 mL) to afford 4-methyl-N-(4-phenoxypyrimidin-2-yl)thiazol-2-amine (0.09 g, 9.40% yield) as a light yellow solid. 1H NMR (CDCl3) δ 8.36 (d, 1H), 7.45 (m, 2H), 7.30 (m, 1H), 7.18 (m, 1H), 7.16 (m, 1H), 6.42 (d, 1H), 6.27 (bs, 1H), 2.30 (d, 3H); Mass spectrum (esi) m/z=385 (100) (M+H1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022222B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-bd636e7d762642e5acc14051737fb665 |
| Source note | uspto-grants-2011_09 |