HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 8-Ethyl-thienyl[3',4':6,5]dipyrido[2,3-b:3',2'-f]azepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 3-(2-Fluoropyridin-3-yl)-4-(2-ethylaminopyridin-3-yl)thiophene | HCID 15408563 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 8-Ethyl-thienyl[3',4':6,5]dipyrido[2,3-b:3',2'-f]azepine | HCID 474620 | — |
Reaction Steps
To a solution of 3-(2-fluoropyridin-3-yl)-4-(2-ethylaminopyridin-3-yl)thiophene (0.021 g) in tetrahydrofuran (1.5 mL was added potassium bistrimethylsilylamide (0.5M in toluene) until no yellow color appeared on addition of further reagent. The mixture was stirred for 5 minutes, ethanol was added, the mixture was diluted with ethyl acetate, washed with water, dried, filtered and evaporated. The residue was fractionated by chromatography to give 8-ethyl-thienyl[3',4':6,5]dipyrido[2,3-b:3',2'-f]azepine mp 140-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919779 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-c63a9319e1304d65a6de669ff8c2c96d |
| Source note | uspto-grants-1999_07 |