A new synthesis of 5-trifluoromethyluracil
P Andres, A Marhold
Index: Andres, Peter; Marhold, Albrecht Journal of Fluorine Chemistry, 1996 , vol. 77, # 1 p. 93 - 95
Full Text: HTML
Citation Number: 21
Abstract
5-Trifluoromethyluracil, an important intermediate for the preparation of the antiviral trifluridine, is obtained by chlorinating thymine to give the new 2, 4-dichloro-5- trichloromethylpyrimidine. Reacting the latter with hydrogen fluoride yields the new 2, 4- difluoro-5-trifluoromethylpyrimidine, and hydrolysis with water gives 5-trifluoromethyluracil in high purity and good yield.
Related Articles:
A facile conversion of 5-trifluoromethyl-5, 6-dihydrouracils to 5-trifluoromethyluracils
[Fuchikami, Takamasa; Yamanouchi, Akiko Chemistry Letters, 1984 , p. 1595 - 1598]
A new synthesis of 5-trifluoromethyluracil
[Journal of Fluorine Chemistry, , vol. 77, # 1 p. 93 - 95]
A new synthesis of 5-trifluoromethyluracil
[Journal of Fluorine Chemistry, , vol. 77, # 1 p. 93 - 95]
A new synthesis of 5-trifluoromethyluracil
[Journal of Fluorine Chemistry, , vol. 77, # 1 p. 93 - 95]