当前位置: X-MOL 学术Bioorg. Med. Chem. Lett. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Synthesis of carbon-11-labeled CK1 inhibitors as new potential PET radiotracers for imaging of Alzheimer’s disease
Bioorganic & Medicinal Chemistry Letters ( IF 2.7 ) Pub Date : 2018-05-29 , DOI: 10.1016/j.bmcl.2018.05.053
Mingzhang Gao , Min Wang , Qi-Huang Zheng

The reference standards methyl 3-((2,2-difluoro-5H-[1,3]dioxolo[4′,5′:4,5]benzo[1,2-d]imidazol-6-yl)carbamoyl)benzoate (5a) and N-(2,2-difluoro-5H-[1,3]dioxolo[4′,5′:4,5]benzo[1,2-d]imidazol-6-yl)-3-methoxybenzamide (5c), and their corresponding desmethylated precursors 3-((2,2-difluoro-5H-[1,3]dioxolo[4′,5′:4,5]benzo[1,2-d]imidazol-6-yl)carbamoyl)benzoic acid (6a) and N-(2,2-difluoro-5H-[1,3]dioxolo[4′,5′:4,5]benzo[1,2-d]imidazol-6-yl)-3-hydroxybenzamide (6b), were synthesized from 5-amino-2,2-difluoro-1,3-benzodioxole and 3-substituted benzoic acids in 5 and 6 steps with 33% and 11%, 30% and 7% overall chemical yield, respectively. Carbon-11-labeled casein kinase 1 (CK1) inhibitors, [11C]methyl 3-((2,2-difluoro-5H-[1,3]dioxolo[4′,5′:4,5]benzo[1,2-d]imidazol-6-yl)carbamoyl)benzoate ([11C]5a) and N-(2,2-difluoro-5H-[1,3]dioxolo[4′,5′:4,5]benzo[1,2-d]imidazol-6-yl)-3-[11C]methoxybenzamide ([11C]5c), were prepared from their O-desmethylated precursor 6a or 6b with [11C]CH3OTf through O-[11C]methylation and isolated by HPLC combined with SPE in 40–45% radiochemical yield, based on [11C]CO2 and decay corrected to end of bombardment (EOB). The radiochemical purity was >99%, and the molar activity (MA) at EOB was 370–740 GBq/μmol with a total synthesis time of ∼40-min from EOB.



中文翻译:

碳11标记的CK1抑制剂的合成作为阿尔茨海默氏病成像的新潜在PET示踪剂

参考标准品甲基3-(((2,2-二氟-5 H- [1,3] dioxolo [4',5':4,5]苯并[1,2 - d ]咪唑-6-基)氨基甲酰基)苯甲酸酯(5a)和N-(2,2-difluoro-5 H- [1,3] dioxolo [4',5':4,5]苯并[1,2- d ]咪唑-6-基)-3 -甲氧基苯甲酰胺(5c)及其相应的脱甲基前体3-((2,2-二氟-5 H- [1,3] dioxolo [4',5':4,5]苯并[1,2- d ]咪唑-6-基)氨基甲酰基)苯甲酸(6a)和N-(2,2-二氟-5 H- [1,3] dioxolo [4',5':4,5]苯并[1,2- d ]咪唑-6-基)-3-羟基苯甲酰胺(6b)由5-氨基-2,2-二氟-1,3-苯并二恶唑和3-取代的苯甲酸分5步和6步合成,总化学收率分别为33%和11%,30%和7%。碳11标记的酪蛋白激酶1(CK1)抑制剂,[ 11 C]甲基3-(((2,2-二氟-5 H- [1,3] dioxolo [4',5':4,5]苯并[ 1,2 - d ]咪唑-6-基)氨基甲酰基)苯甲酸酯([ 11 C] 5a)和N-(2,2-difluoro-5 H- [1,3] dioxolo [4',5':4, 5]苯并[1,2 - d ]咪唑-6-基)-3- [ 11 C]甲氧基苯甲酰胺([ 11 C] 5c)是由其O-去甲基化的前体6a6b具有[ 11 C] CH 3 OTf通过O- [ 11 C]甲基化,并通过HPLC与SPE分离,基于[ 11 C] CO 2的放射化学产率为40-45%,并衰减至轰击结束(EOB) 。放射化学纯度> 99%,在EOB处的摩尔活度(MA)为370–740 GBq /μmol,从EOB的总合成时间约为40分钟。

更新日期:2018-05-29
down
wechat
bug