Triazole alcohol derivative and preparation method and application thereof
A triazole alcohol and triazole technology, applied in the field of pharmaceutical compounds, can solve the problems of narrow antibacterial spectrum, lack of antifungal drugs and deep fungal drugs, and large side effects
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Embodiment 1
[0122] Example 1: (2R,3S)-2-(2,4-difluorophenyl)-3-methyl-1-(1H-1,2,4-triazol-1-yl)-4- Synthesis of Pentyn-2-ol
[0123] Step 1: Synthesis of (R)-3-butyn-2-ol mesylate.
[0124] Dissolve (R)-3-butyn-2-ol (50mmol) in dichloromethane, add triethylamine (100mmol), add methanesulfonyl chloride (55mmol) dropwise at -78°C, after the reaction is complete, pour into an aqueous solution of sodium bicarbonate, extracted twice with dichloromethane, and the organic phase was washed twice with water, dried over anhydrous sodium sulfate, spin-dried and used directly in the next step. 1 H NMR (300MHz, CDCl 3 )δ5.29(q,1H),3.13(s,3H),2.71(s,1H),1.66(d,3H).
[0125] Step 2: Synthesis of (2R,3S)-1-chloro-2-(2,4-difluorophenyl)-3-methyl-4-pentyn-2-ol.
[0126] Pd(CH 3 EN) 2 Cl 2 (5mmol) was dissolved in tetrahydrofuran, triphenylphosphine (12.5mmol) was added, and after 10 minutes of reaction, 2-chloro-2', 4'-difluoroacetophenone (50mmol) and (R)-3-butyne were added -2-alcohol mesylate (5...
Embodiment 2
[0129] Example 2: (2R,3S)-2-(2,5-difluorophenyl)-3-methyl-1-(1H-1,2,4-triazol-1-yl)-4- Synthesis of Pentyn-2-ol
[0130] Step 1: Synthesis of (R)-3-butyn-2-ol mesylate.
[0131] Dissolve (R)-3-butyn-2-ol (50mmol) in dichloromethane, add triethylamine (100mmol), add methanesulfonyl chloride (55mmol) dropwise at -78°C, after the reaction is complete, pour into an aqueous solution of sodium bicarbonate, extracted twice with dichloromethane, and the organic phase was washed twice with water, dried over anhydrous sodium sulfate, spin-dried and used directly in the next step. 1 H NMR (300MHz, CDCl 3 )δ5.29(q,1H),3.13(s,3H),2.71(s,1H),1.66(d,3H).
[0132] Step 2: Synthesis of (2R,3S)-1-chloro-2-(2,5-difluorophenyl)-3-methyl-4-pentyn-2-ol.
[0133] Pd(CH 3 EN) 2 Cl 2 (5mmol) was dissolved in tetrahydrofuran, triphenylphosphine (12.5mmol) was added, and after 10 minutes of reaction, 2-chloro-2', 4'-difluoroacetophenone (50mmol) and (R)-3-butyne were added -2-alcohol mesylate (5...
Embodiment 3
[0136] Embodiment 3: the synthesis of compound 7a
[0137] Dissolve compound 5 (1mmol), compound p-bromobenzotrifluoride (1mmol) in NMP (10mL), add CuI (20mmol%), Pd (PPh3) 2 Cl 2 (5 mmol%), DIEA (5 mmol). Under the protection of nitrogen, react at 60°C for 12h. After TCL monitors that the reaction is complete, extract three times with ethyl acetate, combine the organic phases, wash twice with saturated NaCl, anhydrous NaCl 2 SO 4 dry. After spin-drying, compound 7a was obtained after column chromatography.
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