HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Butyryl-4-(2-methylphenylamino)8-hydroxyquinoline → 3-Butyryl-4-(2-methylphenylamino)-8-(3-morpholinopropoxy)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Butyryl-4-(2-methylphenylamino)8-hydroxyquinoline | HCID 10403732 | — |
| Reactant | 4-(3-Chloropropyl)morpholinium chloride | HCID 12296283 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Butyryl-4-(2-methylphenylamino)-8-(3-morpholinopropoxy)quinoline | HCID 10253053 | 58.1% |
Reaction Steps
3-Butyryl-4-(2-methylphenylamino)-8-hydroxyquinoline (3.2 g, 10 mmol) and potassium t-butoxide (5.0 g, 40 mmol) were stirred in dry dimethylformamide (100 ml) at 100° , then 4-(3-chloropropyl)morpholine hydrochloride (5 0 g, 14 mmol) was added. Heating was continued for 2.5 hours, then the mixture was diluted with water and extracted with ether. The combined extracts were dried and evaporated to an oily residue. Chromatography (silica gel, 3% methanolic ammonia in chloroform) and crystallisation from petroleum ether gave 3-butyryl-4-(2-methylphenylamino)-8-(3-morpholinopropoxy)quinoline (2.6 g, 58 %), m.p. 111°-113°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05082841 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-d36334512b474f208a3726d5f1bda470 |
| Source note | uspto-grants-1992_01 |