HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 3-Bromo-6-methoxypyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | HCID 178508959 | HCID 178508959 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Bromo-6-methoxypyridin-2-amine | HCID 23435879 | 13% |
Reaction Steps
To a solution of 6-amino-5-bromo-pyridin-2-ol (1.0 g) in DMF (30 mL) was added at 0° C. 0.5 M potassium bis(trimethylsilyl)amide in toluene (11.7 mL, 5.83 mmol) under Ar atmosphere. After stirring for 10 minutes, dimethyl sulfate (0.64 mL, 5.26 mmol) was added at 0° C. The mixture was allowed to warm to room temperature, and was stirred for an additional two hours. Buffer (pH 7) was added and mixture was extracted with diethyl ether. The combined organic extracts were washed with brine, dried (Na2SO4), filtered and concentrated to dryness. Purification of the residue by flash chromatography (hexane/toluene 45:55) gave pure 3-bromo-6-methoxy-pyridin-2-ylamine (260 mg, 13% overall).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153809B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-ce2cadbc33ae4ac9b518f9027dcd802b |
| Source note | uspto-grants-2012_04 |