Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 68537762 | HCID 68537762 | — |
| Reactant | HCID 86637898 | HCID 86637898 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68535459 | HCID 68535459 | 32.6% |
Reaction Steps
A mixture of 2-[3-(diphenylmethyl)-6-oxopyridazin-1(6H)-yl]ethyl methanesulfonate (200 mg), ethyl 4-(3-hydroxyphenoxy)butanoate (140 mg), K2CO3 (93 mg), sodium iodide (94 mg), and DMF (2 mL) was stirred at 80° C. for 2 hours. After cooling, the reaction mixture was diluted with EtOAc (50 mL) and washed with water (30 mL) and brine (30 mL) two times. The organic layer was dried over anhydrous MgSO4, filtered and evaporated in vacuo to give crude oil. The crude oil was purified by silica gel column chromatography (n-hexane:EtOAc=1:1) to give ethyl 4-(3-{2-[3-(diphenylmethyl)-6-oxopyridazin-1(6H)-yl]ethoxy}phenoxy)butanoate (87 mg) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08273745B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-5049dbab1632412f9a7a9d7c30b186be |
|---|
| Source note | uspto-grants-2012_09 |
|---|