3430-27-1Relevant articles and documents
Preparation method of (S)-4- (C)-3-(S)-bromopyridine (bromopyridine) (by machine translation)
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Paragraph 0017-0018; 0020-0021; 0023-0024, (2020/02/19)
The method disclosed by the invention has, the beneficial, effects :(1) that 4 - the reaction conditions are mild, the treatment is easy 4 - the method is easy to, operate, the, treatment, is easy . and the method is, easy to, operate 4 - and easy to ;(2) operate 4 - pH, 4 . (by machine translation)
A 4 - methyl -3 - bromo pyridine preparation method
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Paragraph 0014; 0017; 0018; 0020; 0021; 0023; 0024, (2019/06/05)
The invention belongs to the field of organic synthesis, in particular to a 4 - methyl - 3 - bromo pyridine method, comprises the following steps: (1) to 4 - methyl - 3 - nitro pyridine as raw materials, methanol as solvent, under the effects of catalyst hydrogenation reduction, filtered, the filtrate is concentrated, be 4 - methyl - 3 - aminopyridine; (2) the 4 - methyl - 3 - aminopyridine reacts with acid to form the salt cooling to - 10 °C - 0 °C, [...], [...] sodium nitrite aqueous solution, pH adjusting solution is dropped is alkaline, and then extracted, drying, concentration, a 4 - methyl - 3 - bromo pyridine. The beneficial effect of the invention is: mild reaction conditions, is easy to operate, after treatment is simple, and easy to enlarge production, is extremely suitable for industrial production; good catalytic effect, high yield; low prices of raw materials, the production cost is low.
Preparation method for nevirapine intermediate
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Paragraph 0070-0072, (2017/05/27)
The invention relates to a preparation method for an intermediate, i.e., 2-chloro-3-amino-4-methylpyridine, of an anti-AIDs drug nevirapine. The intermediate has a chemical structural formula I as described in the specification. The preparation method is characterized in that 4-methylpyridine is subjected to halogenation, ammonia substitution and chlorination so as to prepare 2-chloro-3-amino-4-methylpyridine. The preparation reactions are as shown in the specifications, wherein X is bromine or chlorine; a halogenation condition is Br2/AlCl3/95-105 DEG C, Br2/AlCl3/MBr/110 to 130 DEG C (wherein M is Li, Na or K), Br2/Fe/135-145 DEG C, Cl2/AlCl3, Br2/FeCl3 or Br2/SnCl4; an ammonia substitution condition is NH3(g)/CuSO4/CH3OH/170-190 DEG C, NH3(aq)/CuSO4/170-190 DEG C, or NaNH2; and a chlorination reaction condition is Cl2/AlCl3 or HCl/H2O2/30-50 DEG C.