HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 5-Bromopyrimidine-2,4-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,4-Diaminopyrimidine | HCID 67431 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Bromopyrimidine-2,4-diamine | HCID 23423590 | 81.6% |
Reaction Steps
To a solution of 2,4-diaminopyrimidine (1.0 g, 9.1 mmol) in chloroform (30 mL) was added N-bromosuccinimide (1.62 g, 9.08 mmol). The solution was stirred in the dark for 12 hours, at which time it was added to CH2Cl2 (150 mL) and 1N NaOH (50 mL). The solid that formed was filtered, rinsed with water and concentrated in vacuo, yielding 1.4 g (74%) of 5-bromopyrimidine-2,4-diamine: LCMS (m/z): 189/191 (MH+); 1H NMR (DMSO-d6): δ 7.78 (s, 1H), 6.58 (bs, 2H), 6.08 (bs, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08173647B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-9a43ddb568854a9d8c1a8774e4f1a516 |
| Source note | uspto-grants-2012_05 |