HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 5-bromo-6-chloro-2-(methylthio)-N-(prop-2-ynyl)pyrimidine-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-chloro-2-(methylthio)-N-(prop-2-ynyl)pyrimidine-4-amine | HCID 90303691 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-bromo-6-chloro-2-(methylthio)-N-(prop-2-ynyl)pyrimidine-4-amine | HCID 90303713 | — |
Reaction Steps
To a stirring solution of 1.16 g (5.45 mmol) of 6-chloro-2-(methylthio)-N-(prop-2-ynyl)pyrimidine-4-amine (intermediate 27) in 6 ml of DCM, 1.07 g (6.0 mmol) of N-bromosuccinimide were added, and stirring was continued for 4 hours at room temperature to give 5-bromo-6-chloro-2-(methylthio)-N-(prop-2-ynyl)pyrimidine-4-amine, which was used without further purification in the next step (see intermediate 31). The completion of the reaction is monitored 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-b8e265fff5ff4cec976cdc1e7c51ab0f |
| Source note | uspto-grants-2016_09 |