HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-3,5-dibromopyrazine → 5-Bromo-3-ethoxypyrazin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-3,5-dibromopyrazine | HCID 620004 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Bromo-3-ethoxypyrazin-2-amine | HCID 12674611 | 87.4% |
Reaction Steps
A solution of 2-amino-3,5-dibromopyrazine (obtained as described in Gazz. Chim. Ital., 1960, 90, 1807) (1.26 g) and sodium ethoxide (0.4 g) in ethanol (50 ml) was heated under reflux for 4 hours. Volatile material was removed by evaporation and the residue was partitioned between water (20 ml) and ethyl acetate (50 ml). The organic layer was separated and dried (MgSO4). Volatile material was removed by evaporation to give 2-amino-5-bromo-3-ethoxypyrazine (0.95 g); 1H NMR (d6 -DMSO): 1.4 (t, 3H), 4.3 (q, 2H), 6.4 (br s, 2H), 7.6 (s, 2H); mass spectrum (+ve CI): 218 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05861401 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-fe396613a8f54efcbe5f8107b1e8dd44 |
| Source note | uspto-grants-1999_01 |