HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4,6-dimethyl pyrimidine → 2-Amino-5-bromo-4,6-dimethylpyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4,6-dimethyl pyrimidine | HCID 13021 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Amino-5-bromo-4,6-dimethylpyrimidine | HCID 2737735 | — |
Reaction Steps
To a stirred solution containing 4.31 g (34.75 mmol) of 2-amino-4,6-dimethylpyrimidine (2) in 150 mL of acetonitrile were added 6.15 g (52.12 mmol) of N-bromosuccinimide. The reaction mixture was stirred at room temperature under argon atmosphere for 3 h. The formed precipitate was filtered and dried to afford the expected product as a white solid: yield 5.93 g (83%). 1H-NMR (CDCl3) δ 5.19 (br, 2H), 2.44 (s, 6H); 13C-NMR (CDCl3) δ 166.28, 160.73, 109.60, 24.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952025B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-c05991a7678c4ab79fee7943cc5faf17 |
| Source note | uspto-grants-2015_02 |