HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,5-Dibromopentane → 4-(3-Chloro-4-(pyridin-2-YL-methoxy)phenylamino)-6-(piperidin-1-YL)-7-(tetrahydrofuran-3-YL-oxy)quinoline-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Amino-4-(3-chloro-4-(pyridin-2-yl-methoxy)phenylamino)-7-(tetrahydrofuran-3-yl-oxy)quinolin-3-carbonitrile | HCID 86694556 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(3-Chloro-4-(pyridin-2-YL-methoxy)phenylamino)-6-(piperidin-1-YL)-7-(tetrahydrofuran-3-YL-oxy)quinoline-3-carbonitrile | HCID 86694557 | — |
Reaction Steps
To a single-neck reaction flask (50 ml) were added 6-amino-4-(3-chloro-4-(pyridin-2-yl-methoxy)phenylamino)-7-(tetrahydrofuran-3-yl-oxy)quinolin-3-carbonitrile (20 mg, 0.041 mmol), anhydrous potassium carbonate powder (10 mg) and chloroform (5 ml). To the flask was added 1,5-dibromopentane (10 mg). The mixture was stirred at the room temperature. After the reaction finished, the mixture was filtered. The filtrate was rotary-evaporated to dryness. The residue was purified with thin layer chromatography (developing solvent: chloroform:methanol=9:1) to give a pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187458B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-0360edb677f349b2ad6195c5c561118d |
| Source note | uspto-grants-2015_11 |