Dipeptidase-IV inhibitor compound
A compound and composition technology, applied in the field of medicine, can solve the problems of not meeting clinical needs, limited variety of DPP-IV inhibitors, etc.
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Embodiment 1
[0146] Example 1 (2R, 5S)-2,5-dihydro-3,6-dimethoxy-2-[bis(4-fluoro-phenyl)]methyl]-5-isopropylpyrazine preparation
[0147]18.4g (100mmol) (2S)-(+)-2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine was dissolved in 400ml tetrahydrofuran, and then heated at -78°C for 30min Add dropwise 48ml (120mmol, 2.5N) of n-butyllithium / n-hexane solution, keep stirring for 30min, then dropwise add 26.3g (110mmol) of 4-fluoro-diphenylchloromethane in 50ml of tetrahydrofuran cold solution, -78°C Stir the reaction for 5h, add 100ml of water at -78°C to quench the reaction, concentrate the reaction solution, partition the residue between ethyl acetate and 1N hydrochloric acid, extract the aqueous layer three times with ethyl acetate, combine the organic layers, wash with salt, and anhydrous Dry over magnesium sulfate, concentrate under reduced pressure, and purify on a silica gel column (ethyl acetate:cyclohexane=1:20~1:10) to obtain 26.8 g of the target compound as colloidal solid, yield: 69.4...
Embodiment 2
[0148] Example 2 Preparation of (R)-N-2-(tert-butoxycarbonyl)-3,3-bis(4-fluorophenyl)alanine methyl ester
[0149] 38.6g (100mmol) of (2R,5S)-2,5-dihydro-3,6-dimethoxy-2-[bis(4-fluoro-phenyl)]methyl]-5-isopropyl Dissolve pyrazine in 200ml of acetonitrile, then add 200ml of 1N hydrochloric acid dropwise, stir the reaction solution at room temperature for 24 hours, add methanol, concentrate to dryness, repeat this operation three times, and then repeat it once with toluene to obtain a solid, which is treated with 700ml of dichloro Add 100g triethylamine after the methane dissolves, then add 52.3g (231.1mmol) (Boc) dropwise 2 O, the reaction solution was stirred at room temperature for 8 h, the solid generated by the reaction was filtered off, the filtrate was diluted with dichloromethane, washed with 1N HCl solution and saturated brine respectively, dried over anhydrous magnesium sulfate, purified on a silica gel column, and the eluents were acetonitrile and petroleum ether (...
Embodiment 3
[0150] Example 3 Preparation of (R)-N-2-(tert-butoxycarbonyl)-3,3-bis(4-fluorophenyl)alanine
[0151] Add 300ml tetrahydrofuran to 23.5g (60mmol) of (R)-N-2-(tert-butoxycarbonyl)-3,3-bis(4-fluorophenyl)alanine methyl ester, cool in an ice bath, and then dropwise add 4.12g (172.3mmol) 200ml aqueous solution of lithium hydroxide, the reaction solution was stirred at room temperature for 15h, concentrated under reduced pressure, the residue was dissolved in ethyl acetate, washed with saturated sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, and evaporated to obtain 18g Solid, yield: 79.3%.
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