HuagongsheHuagongshe Chemistry Print Report · For research reference only
D-Proline → 2-(4-Bromo-3-fluorophenyl)-7-(4-ethoxyphenoxy)imidazo[1,2-b][1,2,4]triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | D-Proline | HCID 8988 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Acetaldehyde, (4-methoxyphenoxy)- | HCID 96383 | — |
| Reactant | 6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amine | HCID 57516523 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(4-Bromo-3-fluorophenyl)-7-(4-ethoxyphenoxy)imidazo[1,2-b][1,2,4]triazine | HCID 68462474 | — |
Reaction Steps
To a cooled (0° C.) mixture of (4-methoxyphenoxy)acetaldehyde (33.2 mg, 0.2 mmol) and D-proline (4.6 mg, 0.04 mmol) in chloroform (1.0 mL) was added N-chlorosuccinimide (26.7 mg, 0.2 mmol) with stirring. The mixture was stirred at 0° C. for 30 min, then gradually warmed to ambient temperature for 2 h. To the reaction mixture was added 6-(4-bromo-3-fluorophenyl)-1,2,4-triazin-3-amine (26.9 mg, 0.1 mmol). The reaction mixture was stirred for 1 h and then the solvent was removed under reduced pressure. The residue was dissolved in isopropanol (2 mL) and heated to 100° C. overnight. After cooling, the mixture was filtered and the filtrate was purified by RP-HPLC (pH 10) to afford the desired product. LCMS: (M+H)=415.0/416.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07767675B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-fd2f9702dba042d9bf06fb42361ac3e2 |
| Source note | uspto-grants-2010_08 |