Analyzing the synthesis route of 2-Chloro-6-methylpyrimidin-4-ylamine

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,14394-60-6, its application will become more common.

Reference of 14394-60-6 ,Some common heterocyclic compound, 14394-60-6, molecular formula is C5H6ClN3, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.

a) 6-methyl-2-(2,2,2-trifluoroethoxy)pyrimidin-4-amine To a stirred solution of 2-chloro-6-methylpyrimidin-4-amine (718 mg, 5.00 mmol, CAS 14394- 60-6) in THF (10 mL) was added NaH (240 mg, 60% in mineral oil, 6.0 mmol) at room temperature. After 30 minutes, 2,2,2-trifluoroethanol (500 mg, 5.00 mmol, CAS 75-89-8) was added and the mixture was heated to 75 C for 16 hours before being partitioned between water and EtOAc. The layers were separated and the organic phase was washed with brine, dried(Na2S04) and concentrated in vacuo to afford the title compound as white solid which was used in the next step without further purification.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,14394-60-6, its application will become more common.

Reference:
Patent; F. HOFFMANN-LA ROCHE AG; HOFFMANN-LA ROCHE INC.; CECERE, Giuseppe; GALLEY, Guido; NORCROSS, Roger; PATINY-ADAM, Angelique; PFLIEGER, Philippe; (68 pag.)WO2016/30306; (2016); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia