Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 68469838 | HCID 68469838 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86627060 | HCID 86627060 | 72% |
Reaction Steps
A solution (0.27 M) of 5-(4-chlorophenyl)-6-cyclohexyl-4-(methoxymethyl)-4H-thieno[3,2-b]pyrrole-2-carboxylic acid in THF was added dropwise to a solution of n-BuLi (3 eq.) and TMEDA (3 eq.) in THF (50 mL) at −78° C. The reaction mixture was stirred at −78° C. for 1.5 h then the resulting solution was treated with DMF (10 eq.). The mixture was stirred at −78° C. for 2 h, then quenched with aqueous NH4Cl (saturated solution), quickly diluted with AcOEt and poured into aqueous HCl (1 N). The aqueous layer was separated and extracted with AcOEt. The combined organic phase was dried and concentrated under vacuum. The resulting residue was azeotropically dried by co-evaporation with toluene, giving a crude that was dissolved in DMF. The resulting solution (0.22 M) was treated with K2CO3 (1.5 eq.) and MeI (5 eq.). The mixture was stirred at RT overnight then diluted with AcOEt and washed with water and brine. Evaporation of the solvent under reduced pressure afforded a residue that was purified by flash chromatography on silica gel (1:9 AcOEt/petroleum ether and AcOEt) to afford the title compound (72%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07781431B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-cf8f14e0621c4bf99fd0c471db5398e3 |
|---|
| Source note | uspto-grants-2010_08 |
|---|