HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 18753199, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 135617196 | HCID 135617196 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18753199 | HCID 18753199 | — |
Reaction Steps
In analogy to the procedure described in example 8, the 6-[4-(4-fluoro-phenyl)-piperazin-1-yl]-2-methyl-5-nitro-3H-pyrimidin-4-one (example 1) was treated with 2-bromo-propane, potassium iodide and potassium carbonate in N,N-dimethylformamide at 80° C. to yield the 4-[4-(4-fluoro-phenyl)-piperazin-1-yl]-6-isopropoxy-2-methyl-5-nitro-pyrimidine as a light yellow solid; m.p. 98-100° C.; MS: [M+H]+=376.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06673795B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-62eb4f0e15fd4ebaa6020093cc2fc182 |
| Source note | uspto-grants-2004_01 |