New downstream synthetic route of 56621-48-8

Although many compounds look similar to this compound(56621-48-8)Synthetic Route of C10H14N2O, numerous studies have shown that this compound(SMILES:OC1=CC=C(N2CCNCC2)C=C1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Synthesis, Radiofluorination, and In Vitro Evaluation of Pyrazolo[1,5-a]pyridine-Based Dopamine D4 Receptor Ligands: Discovery of an Inverse Agonist Radioligand for PET, published in 2008-03-27, which mentions a compound: 56621-48-8, mainly applied to pyrazolopyridine arylpiperazinylmethyl preparation radiofluorination dopamine receptor radioligand, Synthetic Route of C10H14N2O.

A series of fluoro-substituted analogs structurally derived from the aminomethyl-substituted pyrazolo[1,5-a]pyridine lead compounds FAUC 113 and FAUC 213 were synthesized and evaluated as high-affinity D4 receptor (D4R) ligands (Ki = 1.3-28 nM). The para-fluoroethoxy-substituted derivatives I and II revealed an outstanding D4 subtype selectivity of more than 3 orders of magnitude over both congeners D2 and D3 combined with inverse agonism at D4R. The corresponding 18F-labeled radioligands revealed high serum stability in vitro and log P values of 2-3. In vitro rat brain autoradiog. showed specific binding of [18F]-II in distinct brain regions, including the gyrus dentate of the hippocampus, that were inhibited by both eticlopride (65-80%) and the selective D4R antagonist 10 (78-93%). The observed binding pattern was mainly consistent with the known D4R distribution in the rat brain. Thus, [18F]-II (FAUC F41) represents a potential radioligand for studying the D4R in vivo by positron emission tomog. (PET).

Although many compounds look similar to this compound(56621-48-8)Synthetic Route of C10H14N2O, numerous studies have shown that this compound(SMILES:OC1=CC=C(N2CCNCC2)C=C1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem