A kind of positron imaging agent targeting ASGPR and its preparation method and application
A positron imaging agent, targeting technology, applied in the preparation of sugar derivatives, organic chemistry methods, chemical instruments and methods, etc., can solve false positives, multimer synthesis difficulties, probe targeting and insufficient affinity and other problems, to achieve the effect of strong affinity and good imaging effect
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[0035] The preparation method of the above-mentioned positron imaging agent targeting ASGPR comprises the following steps:
[0036] 1) Disperse 4-pentyn-1-ol in a solvent, then add triethylamine, 4-dimethylaminopyridine and p-toluenesulfonyl chloride, fully react, extract the reaction solution, and then remove water from the extract , vacuum distillation and column chromatography to obtain
[0037] 2) Will dispersed in a solvent, and then added 18 F ions, fully reacted, get
[0038] 3) Will Disperse in the solvent, then add 4A molecular sieve, mix evenly, then add trimethylsilane azide and tin tetrachloride, fully react, remove 4A molecular sieve by suction filtration, then dewater the filtrate, vacuum distillation and column layer analyzed and separated to obtain
[0039] 4) Will Disperse in a solvent, then add sodium methoxide, fully react, adjust the pH value of the reaction solution to 6-7, filter and dry to obtain
[0040] 5) Will dispersed in a solven...
Embodiment 1
[0057] A preparation method of a positron imaging agent targeting ASGPR, comprising the following steps:
[0058] 1) Disperse 4-pentyn-1-ol (2.52g, 30mmol) in 80mL of dichloromethane, then add triethylamine (10.12g, 100mmol), 4-dimethylaminopyridine (0.16g, 1.32mmol) and p-toluenesulfonyl chloride (6.86g, 36mmol), reacted at room temperature for 14h, then extracted with ethyl acetate, and then subjected to anhydrous sodium sulfate dehydration, vacuum distillation and column chromatography to separate the extract to obtain a light yellow liquid Yield 39%; 1 H NMR (600MHz, CDCl 3 )δ7.80(d, J=8.3Hz, 2H), 7.35(d, J=8.1Hz, 2H), 4.15(t, J=6.1Hz, 2H), 2.44(d, J=13.4Hz, 3H) ,2.26(dt,J=6.9,2.6Hz,2H),1.86(m,2H),1.23(m,1H);
[0059] 2) Will (35.7mg, 0.15mmol) was dispersed in 1mL acetonitrile, then added 18 F ions (100mCi), reacted at 85°C for 10min to obtain Yield 40%;
[0060] 3) Will (3.9g, 10mmol) was dispersed in 20mL of ultra-dry dichloromethane, then an appropriate amo...
Embodiment 2
[0069] A preparation method of a positron imaging agent targeting ASGPR, comprising the following steps:
[0070] 1) Disperse 4-pentyn-1-ol (2.52g, 30mmol) in 80mL of dichloromethane, then add triethylamine (10.12g, 100mmol), 4-dimethylaminopyridine (0.16g, 1.32mmol) and p-toluenesulfonyl chloride (6.86g, 36mmol), reacted at room temperature for 12h, then extracted with ethyl acetate, and then subjected to anhydrous sodium sulfate dehydration, vacuum distillation and column chromatography to separate the extract to obtain a light yellow liquid Yield 36%;
[0071] 2) Will (35.7mg, 0.15mmol) was dispersed in 1mL acetonitrile, then added 18 F ions (100mCi), reacted at 85°C for 15min to obtain Yield 38%;
[0072] 3) Will (3.9g, 10mmol) was dispersed in 20mL of ultra-dry dichloromethane, then an appropriate amount of freshly evaporated 4A molecular sieves was added, stirred for 20min, then trimethylsilyl azide (1.38g, 12mmol) and tin tetrachloride ( 4.168g, 16mmol), stirr...
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