HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 5-Bromo-4-methylpyrimidin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Amino-4-methylpyrimidine | HCID 7939 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Bromo-4-methylpyrimidin-2-amine | HCID 18616196 | 100% |
Reaction Steps
To a solution of 4-methylpyrimidine-2-ylamine (10.9 g, 100 mmol) in chloroform (400 mL) was added N-bromosuccinimide (17.8 g, 100 mmol). The solution was stirred in the dark for 15 hours, at which time it was added to CH2Cl2 (1400 mL), washed with 1N NaOH (3×200 mL) and NaCl(sat.) (100 mL), dried over Na2SO4, filtered and concentrated, yielding 5-bromo-4-methylpyrimidine-2-ylamine (18.8 g, 99%). LCMS (m/z): 188.0/190.0 (MH+). 1H NMR (CDCl3): δ 8.22 (s, 1H), 5.02 (bs, 2H), 2.44 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08563549B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-ceb63e74e2ad4ce98e328f5fce0de40e |
| Source note | uspto-grants-2013_10 |