HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Benzyloxy-N-(2,5-dibromo-pyridin-3-yl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyloxyacetyl chloride | HCID 177085 | — |
| Reactant | 2,5-Dibromopyridin-3-amine | HCID 19387532 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Benzyloxy-N-(2,5-dibromo-pyridin-3-yl)-acetamide | HCID 59402684 | 24.17% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To the solution of 2,5-Dibromo-pyridin-3-ylamine (8.6 g, 34.12 mmol) in 50 ml of DCM was added triethylamine (5.3 ml, 37.53 mmol). Cooled the reaction mixture to 0° C. To this added the solution of 2-benzyloxy acetyl chloride (7.45 g, 40.95 mmol) in 35 ml of DCM. The reaction mixture was stirred at 25° C. for 12 hr. After the completion of the reaction mixture (TLC monitoring), the reaction mixture was evaporated to dryness under reduced pressure. The residue was purified by column chromatography on silica (60-120 M) using ethyl acetate/hexane (10:90) as the eluent to provide the title compound (3.2 g, 24.17%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088791B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-d1b73028994d4389a2224ada59a3b93a |
| Source note | uspto-grants-2012_01 |