HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 67266527, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | (4-Ethynylphenyl)methanol | HCID 11170993 | — |
| Reactant | HCID 57826288 | HCID 57826288 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Product | HCID 67266527 | HCID 67266527 | — |
Reaction Steps
7-(2,6-Dibromo-pyridin-4-ylsulfanyl)-2-methyl-phenoxy}-acetic acid methyl ester (0.3 g; 0.67 mmol, prepared as described in example 6), cupper iodide (3.8 mg; 0.02 mmol), 4-ethynylbenzylalcohol (266 mg; 2.01 mmol) and bis(triphenylphosphine) palladium (II) chloride (18.8 mg; 0.027 mmol) were added to a dry reaction flask under an atmosphere of nitrogen. Triethylamine (2 ml) and DMF (2 ml) was added and the reaction mixture was reacted at 70° C. for 10 min in a microwave oven. The reaction mixture was purified by preparative HPLC (method B) to give {4-[2,6-bis-(4-hydroxymethyl-phenylethynyl)-pyridin-4-ylsulfanyl]-2-methyl-phenoxy}-acetic acid methyl ester. Yield: 260 mg; 70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07968723B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-e25d93e5c67344b9baa7ce4804400122 |
| Source note | uspto-grants-2011_06 |