A kind of alanine derivative and its preparation method and application
A derivative, alanine technology, applied in the field of alanine derivatives and its preparation, can solve problems such as adverse reactions and drug resistance, and achieve the effect of improving affinity and good space matching
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[0030] see figure 1 , as the preparation method of the alanine derivative of above-mentioned structure, comprises the following steps:
[0031] 1) 5-bromo-2-aminopyridine is acylated with an acid chloride compound to prepare acylated 5-bromo-2-aminopyridine;
[0032] 2)N 2 Under protection, 5-bromonicotinic acid, thionyl chloride and amine compounds react to prepare ammoniated 5-bromonicotinic acid;
[0033] 3) Under the catalysis of tetrakistriphenylphosphine palladium, acylated 5-bromo-2-aminopyridine or ammoniated 5-bromonicotinic acid and m-carboxyphenylboronic acid undergo Suzuki coupling reaction to obtain pyridine-benzene compound;
[0034] 4) Boc-L-alanine is condensed with 3-trifluoromethyl-4-chloroaniline to generate tert-butyl-(R)-(1-((4-chloro-3-(trifluoromethyl)phenyl )amino)-1-oxypropan-2-yl)carbamate;
[0035] 5) tert-butyl-(R)-(1-((4-chloro-3-(trifluoromethyl)phenyl)amino)-1-oxypropan-2-yl)carbamate removes Boc protection The base generates (R)-2-amino-N-(...
Embodiment 1
[0046] A kind of alanine derivative, is characterized in that, R is , the preparation method is as follows:
[0047] 1) Synthesis of N-(5-bromopyridin-2-yl)acetamide: 5-bromo-2-aminopyridine (5.19 g, 30 mmol) was dissolved in 100 ml of anhydrous dichloromethane, and 20 ml of triethylamine was added. Under the condition of ice bath, acetyl chloride (2.54ml) was slowly added dropwise to the above solution. After the dropwise addition was completed, the ice bath was removed, and the mixture was raised to room temperature to react overnight. After the reaction was finished, dichloromethane was added for dilution, washed with water (30ml×3), saturated NaHCO 3 Solution washing (30ml×3), saturated NaCl washing (30ml), organic phase anhydrous NaCl 2 SO 4 dry. Column chromatography separated 5.65 g of white solid with a yield of 88%. Mp 78-81℃; EI-MS(m / z):214[M] + .
[0048] 2) Synthesis of 3-(6-(acetylamino)pyridin-3-yl)benzoic acid: N-(5-bromopyridin-2-yl)acetamide (4.30g, 20...
Embodiment 2
[0054] A kind of alanine derivative, is characterized in that, R is , the preparation method is as follows:
[0055] 1) Synthesis of 5-bromo-N-cyclopropyl nicotinamide: in N 2Under protection, add thionyl chloride (36ml, 494mmol) dropwise to 5-bromonicotinic acid (5.00g, 24.7mmol). After the dropwise addition, heat to reflux for 2-3h until the solution is clear, and spin off the chloride under reduced pressure. Sulfoxide, a light yellow solid was obtained. The solid was dissolved in 30ml of anhydrous dichloromethane, and the reactive intermediate solution was slowly added dropwise to a solution of cyclopropylamine (3.77ml) in dichloromethane (30ml) under ice-bath conditions. After the dropwise addition, it was raised to room temperature and reacted overnight. After the reaction, add 2mol / L K to the reaction system 2 CO 3 Solution 20ml. Separate the liquid to take the dichloromethane phase, extract the aqueous phase with dichloromethane (15ml × 3), combine the organic ph...
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