HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 5-Bromo-6-chloro-2-(methylsulfanyl)pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 15563630 | HCID 15563630 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-6-chloro-2-(methylsulfanyl)pyrimidin-4-amine | HCID 12369427 | — |
Reaction Steps
To a cold stirring solution of 10 g (52.2 mmol) 6-chloro-2-(methylsulfinyl)pyrimidine-4-amine in 450 ml of DCM, 10 g (56.2 mmol) of N-bromosuccinimide were added, and stirring was continued for 1 hour at room temperature to provide 5-bromo-6-chloro-2-(methylthio)pyrimidine-4-amine, which was used without further purification in the next step (see intermediate 3). The end of the reaction is followed by thin layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447095B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-b6e875bc27c641fda5fef35ae7d10504 |
| Source note | uspto-grants-2016_09 |