Synthesis
General procedure: A mixed solution of 5-amino-4,6-dichloropyrimidine (1.0 mmol), triethylamine (1.0 mmol), ethanol (4.3 mL) and n-propylamine (2.5 mmol) was placed in an autoclave reactor, heated to a specified temperature and kept for a period of time. After completion of the reaction, the volatile components were evaporated under reduced pressure and the crude product was purified according to a specific method to obtain the target compound 6-chloro-N4-propyl-4,5-pyrimidinediamine.
References
[1] European Journal of Medicinal Chemistry, 2018, vol. 151, p. 199 - 213
[2] Journal of Medicinal Chemistry, 1997, vol. 40, # 20, p. 3207 - 3216
[3] Patent: WO2014/75393, 2014, A1. Location in patent: Page/Page column 175
[4] Organic Letters, 2017, vol. 19, # 23, p. 6360 - 6363
