HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-Amino-5-bromo-4-methoxypyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Methoxy-2-pyrimidinamine | HCID 67428 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Amino-5-bromo-4-methoxypyrimidine | HCID 45036937 | 96% |
Reaction Steps
To a solution of 4-methoxypyrimidine-2-ylamine (1.84 g, 14.7 mmol) in chloroform (600 mL) was added N-bromosuccinimide (2.62 g, 14.7 mmol). After stirring in the dark for 5 hours, the solution was added to CH2Cl2 (200 mL) and 1N NaOH (100 mL). Upon mixing, the layers were separated and the organic layer was washed with NaCl(sat.) (100 mL), dried over Na2SO4, filtered and concentrated yielding 2.88 g (96%) of 5-bromo-4-methoxypyrimidine-2-ylamine. LCMS (m/z): 204/206 (MH+). 1H NMR NMR (CDCl3): δ 8.10 (s, 1H), 4.93 (bs, 2H), 3.96 (s, 31-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08563549B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-a145154cd71d414a8031322f61d46659 |
| Source note | uspto-grants-2013_10 |