Reaction #710481
ord-af4cb05f4ccf4c029efb5271f7ccee41
Reaction equation
2-chloro-5-chloromethyl pyridine
2-aminopyrimidine
→
1-((6-chloropyridin-3-yl)methyl)pyrimidin-2(1H)-imine hydrochloride
Yield 34.0%
Reagents
None
Solvents
Conditions
Temperature
80°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1Otherwas returned to room temperature
- 2workup.DISTILLATIONto distill off DMF under reduced pressure
- 3workup.ADDITIONDiethyl ether was added
- 4Otherthus crystallization
- 5Otherwas occurred on the wall surface of an eggplant flask
- 6OtherDiethyl ether was removed by decantation
- 7Otherdried well
Procedure
300 mg (1.86 mmol) of 2-chloro-5-chloromethyl pyridine was dissolved in 6 ml of anhydrous DMF, 118 mg (1.24 mmol) of 2-aminopyrimidine was added thereto, and the resulting mixture was stirred at 80° C. for 8 hours. After the reaction was completed, the reaction solution was returned to room temperature to distill off DMF under reduced pressure. Diethyl ether was added thereto, and thus crystallization was occurred on the wall surface of an eggplant flask. Diethyl ether was removed by decantation and dried well to obtain 1-((6-chloropyridin-3-yl)methyl)pyrimidin-2(1H)-imine hydrochloride. Amount obtained 107 mg (yield 34%)