Preparation method of 1,4,5-trisubstituted-2-aminoimidazole compounds
An aminoimidazole and compound technology, which is applied in the field of preparation of 1,4,5-trisubstituted-2-aminoimidazole compounds, can solve the problems of poor applicability of different functional groups, complicated operation, expensive operation of alkyne and silver nitrate, etc. The reaction raw materials are cheap and easy to obtain, the raw materials are cheap and easy to obtain, and the conditions are mild.
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Embodiment 1
[0042] Example 1: Preparation of 5-(4-chlorophenyl)-1-(4-methylphenyl)-4-methyl-1H-imidazol-2-amine
[0043] 1. Raw material 1: Preparation of 3-(4-chlorophenyl)-2-methyl-2-nitrooxirane
[0044] Add 2.8g (20mmol) of p-chlorobenzaldehyde and 9.0ml (100mmol) of nitroethane into a three-necked flask, and slowly add Et 3 N0.28ml (2mmol), after the addition is complete, stir at room temperature under nitrogen protection for 18h. After the TLC plate detects that the raw material disappears, the excess solvent is evaporated under reduced pressure, and the crude product α-nitroalcohol is directly dissolved in dichloromethane, and then 7.4 mL (42 mmol) of N,N-diisopropylethylamine and methyl Sulfonyl chloride 1.9mL (24mmol), after the addition, the reaction gradually returned to room temperature. After the TLC plate detected that the raw materials disappeared, the reaction system was extracted with dichloromethane. The organic phase was washed twice with 10ml of 2M dilute hydrochloric...
Embodiment 2
[0066] Preparation of Example 2, 5-(4-chlorophenyl)-1-(4-methoxyphenyl)-4-methyl-1H-imidazol-2-amine
[0067] Replace p-methylaniline with p-methoxyaniline, the molar weight is constant, and all the other are the same as in Example 1. 297 mg of the product 5-(4-chlorophenyl)-1-(4-methoxyphenyl)-4-methyl-1H-imidazol-2-amine was obtained as a yellow solid, with a yield of 95%.
[0068] Its structural formula is:
[0069]
[0070] 1 HNMR (500MHz, CDCl 3 )δ7.18(d,J=8.5Hz,2H),7.09(d,J=8.8Hz,2H),6.94(d,J=8.5Hz,2H),6.91(d,J=8.8Hz,2H) ,4.18(s,1H),3.83(s,3H),2.24(s,3H). 13 CNMR (126MHz, CDCl 3 ) 13 CNMR (125MHz, CDCl 3 )δ159.21, 148.10, 132.11, 131.78, 130.04, 129.35, 128.58, 128.56, 128.30, 122.99, 114.95, 55.48, 13.53 HRMS (ESI): m / zcalcdforC 17 h 17 ClN 3 O[M+H] + :314.1060,found:314.1058.
Embodiment 3
[0071] The preparation of embodiment 3, 5-(4-chlorophenyl)-1-phenyl-4-methyl-1H-imidazol-2-amine
[0072] Replace p-methylaniline with aniline, the molar weight is constant, and all the other are the same as in Example 1. 255 mg of the product 5-(4-chlorophenyl)-1-(4-methoxyphenyl)-4-methyl-1H-imidazol-2-amine was obtained as a yellow solid, with a yield of 90%.
[0073] Its structural formula is:
[0074]
[0075] 1 HNMR (500MHz, CDCl 3 )δ7.44-7.40(m,2H),7.39-7.35(m,1H),7.20-7.14(m,4H),6.93(d,J=8.5Hz,2H),4.30(s,2H),2.24 (s,3H). 13 CNMR (125MHz, CDCl 3 )δ147.8, 135.82, 132.01, 131.92, 130.06, 129.87, 129.05, 128.35, 128.32, 127.29, 122.78, 13.29; HRMS (ESI): m / zcalcdforC 16 h 15 ClN 3 [M+H] + :284.0955,found:284.0951.
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