Diethylcarbamyl-substituted thiazole dihydropyrimidine
A thiazole, oxo technology, applied in the treatment and prevention of HBV infection, the application field of treatment and prevention of hepatitis B virus infection, can solve the problems of side effects, rebound effect and so on
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Embodiment 1
[0133] Ethyl 4-(2-chloro-4-fluorophenyl)-2-(thiazol-2-yl)-6-methyl-1,4-dihydropyrimidine-5-carboxylate
[0134]
[0135] 10.0g (63.1mmol) of2-chloro-4-fluorobenzaldehyde, 8.2g (63.1mmol) ethylacetoacetic acid, 10.3g (63.1mmol) 2-amidino-thiazole hydrochloride and 6.2g (75.7mmol) acetic acid Sodium was dissolved or suspended in 500ml of ethanol and boiled under reflux for 16 hours. Cool to room temperature, filter with suction, and wash the residue with water to remove inorganic salts. 12.8 g (53.4%) of product were obtained, melting point: 162-164°C.
Embodiment 2
[0137] Methyl 4-(2-chloro-4fluorophenyl)-2-(thiazol-2-yl)-6-methyl-1,4-dihydropyrimidine-5-carboxylate
[0138] The compound was synthesized using methyl acetoacetic acid according to a method similar to Example 1.
[0139] Yield: 55% (melting point: 152-154°C)
Embodiment 3
[0141] Ethyl 4-(2-bromo-4fluorophenyl)-2-(thiazol-2-yl)-6-methyl-1,4-dihydropyrimidine-5-carboxylate
[0142] The compound was synthesized using ethyl acetoacetic acid according to a method similar to Example 1.
[0143] Yield: 51.6% (melting point: 163-165°C)
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