Method for synthesizing antitumor compound of diketopiperazine PJ147
A technology of PJ147 and diketopiperazine, which is applied in the field of synthesis of anti-tumor compound diketopiperazine PJ147, achieving the effect of high yield and low cost
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Embodiment 1
[0025] Embodiment 1: the preparation of glycoside dipeptide
[0026] Dissolve L-alanine methyl ester (1.19g, 10mmol), triethylamine (1.01g, 10mmol) in dichloromethane (10ml), add N-benzyloxycarbonyl-L-glycine (2.09g, 10mmol) and HOBt (1-hydroxybenzotriazole) (1.35g, 10mmol), cooled to 0°C, added 10ml of DCC (N, N'-dicyclohexylcarbodiimide) (2.07g, 10mmol) Chloromethane solution, stirring and reacting at this temperature for 4 hours, continuing to react at room temperature for 8 hours, concentrating under reduced pressure, dissolving the residue in 20ml of ethyl acetate, diluting with 20ml of 2% hydrochloric acid, 20ml of 5% sodium bicarbonate solution and 20ml of Washed with water, dried over anhydrous sodium sulfate, distilled under reduced pressure, and recrystallized with ethyl acetate-petroleum ether-ether to obtain protected glycinyl methyl ester (N-benzyloxycarbonyl-L-glycerol-L-propan-OCH 3 ) 2.82g. N-Benzyloxycarbonyl-L-glycerin-L-propane-OCH 3 Dissolve in methanol ...
Embodiment 2
[0027] Embodiment 2: the preparation of 4-geranyloxybenzaldehyde
[0028] P-Hydroxybenzaldehyde (3.32g, 27mmol) and anhydrous potassium carbonate (4.42g, 32mmol) were dissolved in 10ml of anhydrous acetone, and bromogeraniol (5.40g, 25mmol) was slowly added dropwise under stirring at room temperature, and stirred for 5 hour, filter with suction, evaporate acetone under reduced pressure, add 50ml of ethyl acetate, wash the ethyl acetate layer with 50ml of 10% potassium hydroxide solution and water successively, dry over anhydrous sodium sulfate, filter overnight, and evaporate ethyl acetate under reduced pressure , 5.30 g of 4-geranyloxybenzaldehyde was obtained with a yield of 82%. 1 H-NMR (300MHz, DMSO-d 6 ): 1.62 (3H, s), 1.70 (3H, s), 1.76 (3H, s), 2.08 (2H, m), 2.13 (2H, m), 4.60 (2H, d, J=6.5Hz), 5.10 (1H, m), 5.50 (1H, t, J = 6.5Hz), 6.98 (2H, d, J = 8.7Hz), 7.78 (2H, d, J = 8.7Hz), 8.62 (1H, s).
Embodiment 3
[0029] Embodiment 3: the preparation of diketopiperazine PJ147
[0030] Take 128mg (1mmol) of proglycerin dipeptide, add it to 4ml of acetic anhydride, react overnight at 130°C, remove the acetic anhydride under reduced pressure, add a small amount of water to evaporate the remaining acetic anhydride at low temperature and reduce pressure, dissolve the product in 5ml of DMF, add 4- Geranyloxybenzaldehyde (920mg, 4mmol) DMF solution 5ml, 5ml t-BuOK solution in tert-butanol (containing t-BuOK 0.11g, 1mmol) was added dropwise, stirred at room temperature for 5 hours, filtered, evaporated under reduced pressure Solvent, dissolved in 10ml DMF, filtered, added hydrazine hydrate (0.25ml, 4mmol) to the filtrate, stirred at room temperature for 3 hours, and filtered to obtain 280mg of white precipitate, which was the target product diketopiperazine PJ147, with a yield of 76%. 1 H-NMR (300MHz, DMSO-d 6 ): 1.32 (3H, d, J=6.9Hz), 1.57 (3H, s), 1.63 (3H, s), 1.71 (3H, s), 2.06 (2H, m), 2....
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