Small molecular inhibiting agent for coronavirus main proteinase, its preparation method and uses
A compound, free technology, applied in the direction of antiviral agents, peptide/protein components, medical preparations containing active ingredients, etc., to achieve the effect of good application prospects
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[0067] The preparation method of the compound of the present invention
[0068] The preparation method of the compound of formula (I) provided by the present invention comprises the following steps:
[0069] The protecting group R of the amino group in the formula (II) compound 6 removed, where the R 6 selected from the group consisting of the following groups: tert-butoxycarbonyl, trifluoroacetyl, benzyloxycarbonyl;
[0070] In the presence of a condensation reagent, the product of the previous step is condensed with a compound of formula (III) to obtain a compound of formula (I),
[0071]
[0072]
[0073]
[0074] Wherein, R in formula (II) and formula (III) 1 , R 2 , R 4 , the definition of U is the same as that in formula (I).
[0075] The synthesis of the compound of formula (II) can refer to: Qingping Tian, Naresh K.Nayyar, Srinivasan Babu, Lijian Chen, Junhua Tao, Steven Lee, Anthony Tibbetts, Terence Moran, Jason Liou, Ming Guo and Timothy P.Kennedy...
Embodiment 1
[0082] 42mg of Dissolve in 2 ml of CH 2 Cl 2 , add 0.5ml of TFA to react at room temperature for 1 hour, and drain the solvent. The resulting de-Boc substrate was dissolved in 2 ml of CH 2 Cl 2 In, add 40mg of Then add 71 μl of i PR 2 NEt, then add 63mg of HATU. React at room temperature for 12 hours, successively wash with 1M HCl, saturated NaHCO 3 aqueous solution, saturated brine washing, Na 2 SO 4 dry. Filtration, evaporation of the solvent under reduced pressure, and flash column chromatography gave 52 mg of the product Yield 80%.
[0083] The spectrogram data is as follows:
[0084] H NMR: δ (500MHz, CDCl 3)0.76(d, 3H, J=6.9Hz), 0.98(d, 3H, J=5.7Hz), 1.30(t, 3H, J=7.3Hz), 1.42(s, 9H), 1.74-1.94(m, 4H), 2.10-2.40(m, 2H), 2.49-2.52(m, 1H), 2.67-2.71(m, 1H), 2.85-3.00(m, 1H), 3.05-3.17(m, 1H), 3.23- 3.39(m, 3H), 4.18(q, 2H, J=7.1Hz), 4.41-4.51(m, 1H), 4.58-4.65(m, 1H), 5.03-5.10(m, 1H), 5.49(t, 1H, J=14.7Hz), 5.98(dd, 1H, J=15.8Hz, 4.4Hz), 6.70-7.00(m, 3...
Embodiment 2
[0088] 45mg Dissolve in 2 ml of CH 2 Cl 2 , add 0.5ml of TFA to react at room temperature for 1 hour, and drain the solvent. The resulting de-Boc substrate was dissolved in 2 ml of CH 2 Cl 2 , add 12mg of Then add 48 μl of i PR 2 NEt, then add 44mg of HATU. React at room temperature for 12 hours, successively wash with 1M HCl, saturated NaHCO 3 aqueous solution, saturated brine washing, Na 2 SO 4 dry. Filtration, evaporation of the solvent under reduced pressure, and flash column chromatography gave 34 mg of the product Yield 73%.
[0089] The spectrogram data is as follows:
[0090] H NMR: δ (300MHz, CDCl 3 )0.85(d, 3H, J=6.6Hz), 1.03(d, 3H, J=6.9Hz), 1.30(t, 3H, J=7.2Hz), 1.52-1.61(m, 1H), 1.71-1.90( m, 2H), 2.26-2.42(m, 2H), 2.48(s, 3H), 2.53-2.73(m, 3H), 2.84-2.98(m, 2H), 3.13-3.23(m, 1H), 3.30- 3.42(m, 2H), 4.18(q, 2H, J=7.2Hz), 4.41-4.56(m, 1H), 4.66-4.76(m, 1H), 5.50(d, 1H, J=15.6Hz), 5.91 (s, 1H), 6.39 (s, 1H), 6.63 (dd, 1H, J = 15.3Hz, 4.8Hz), 6.94...
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