Anticancer intermediate based on PKI-587 and polyethylene glycol coupled anticancer drug, and preparation methods and application thereof
A technology of PKI-587 and anti-cancer drugs, which is applied in the field of cancer treatment, can solve problems such as the limitation of clinical efficacy, achieve significant clinical value, reduce toxicity, and have a broad market prospect
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[0081] The above-mentioned preparation method of the anticancer intermediate shown in formula I, it comprises:
[0082] Step S1: Amidation reaction of PKI-587 with amino acid or peptide and its derivatives to obtain the first intermediate having the N-AC structural unit in the formula I; At least one of the anticancer drugs undergoes an amidation reaction with amino acids or peptides and derivatives thereof to obtain another first intermediate having the N-AC structural unit in the formula I.
[0083] Preferably, the synthesis method of the first intermediate comprises: after amidation linking the amino acid or polypeptide with an amino protecting group and its derivatives with an anticancer drug in the presence of a polypeptide condensation reagent, deprotecting the amino group .
[0084] Wherein, the polypeptide condensation reagent includes HBTU, HOBT, HBTU. The alkaloid DIEA (N,N-diisopropylethylamine) is also added in the reaction, and the reaction temperature is -10-10...
Embodiment 1-1
[0121] preparation:
[0122] Glycine (11.1194g, 148.12mmol) was added to a 1L round bottom flask, 1,4-dioxane (150ml) was added to dissolve it, magnetons were added, 2N NaOH (88.88ml, 177.78mmol) was added, and Boc Anhydride (48.5 g, 222.22 mmol). After the reaction was completed, the reaction liquid was transferred to a rotary evaporator for concentration, and the concentrated liquid was transferred to a 1L separatory funnel, and 100 ml of diethyl ether was added for washing, and the reaction was repeated twice. Separate the aqueous phase and the organic phase, and add 1 mol / L hydrochloric acid to the aqueous phase to adjust the pH to pH=4. Extract the aqueous phase (150ml×5) with ethyl acetate, combine the organic phases, add anhydrous sodium sulfate to the organic phases to dry, filter with suction, remove water with toluene, and evaporate to dryness to obtain Compound A with a yield of 100%.
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