HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hexamethyldisilazide → 6-Methoxyquinolin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 3-Bromo-6-methoxyquinoline | HCID 14758587 | — |
| Reactant | Tri-t-butylphosphine fluoroborate | HCID 44558591 | — |
| Catalyst | Tris(dibenzylideneacetone) dipalladium | HCID 9832798 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-Methoxyquinolin-3-amine | HCID 599939 | — |
Reaction Steps
To a stirred mixture of 3-bromo-6-methoxyquinoline [synthesis given in Tetrahedron (1986), 42, 1475-1485] (2.38 g), tris(dibenzylideneacetone) dipalladium (0) (0.114 g) and tri t-butylphosphine tetrafluoroborate (0.116 g) in toluene (15 ml) under an atmosphere of nitrogen at ambient temperature was added a solution of lithium bistrimethylsilylamide (11.0 ml, 1.0M solution in hexanes). The mixture was stirred for 2 days and the brown suspension diluted with diethyl ether and extracted with 2M aqueous hydrochloric acid (twice) and the acidic fractions combined, washed with diethyl ether and made basic with 2M aqueous sodium hydroxide to give the required product as a brown solid that was used in the next Step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07956188B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-36099860a7fe437e914e14a1229bfd85 |
| Source note | uspto-grants-2011_06 |