Extracurricular laboratory:new discovery of 2-Fluoro-5-((4-oxo-3,4-dihydrophthalazin-1-yl)methyl)benzoic acid

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 763114-26-7

Related Products of 763114-26-7, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.763114-26-7, Name is 2-Fluoro-5-((4-oxo-3,4-dihydrophthalazin-1-yl)methyl)benzoic acid, molecular formula is C16H11FN2O3. In a Patent£¬once mentioned of 763114-26-7

A phthalazinone derivative and its preparation method and medical use (by machine translation)

The present invention provides a phthalazinone derivative and its preparation method and medical use. In order to O-aldehyde benzoic acid as the raw material, by reaction with methyl (3 – oxo – 1, 3 – ISO-benzofuran – 1 – yl) phosphonic acid dimethyl ester, the compound with 3 – cyano – 4 – fluorophenyl with formaldehyde in the presence of triethylamine to produce (Z, E) – 2 – fluoro – 5 – [(3 – oxoisoindoline benzofuran – 1 (3 H) – ylidene) methyl] benzonitrile, it is hydrazine hydrate is reduced to 2 – fluoro – 5 – [(4 – oxo – 3, 4 – […] – 1 – yl) methyl] benzoic acid; benzene formaldehyde or substituted aryl formaldehyde or furfural as raw materials, with malonic acid in the Knoevenagel reaction, the obtained acrylic acid or substituted the acrylic acid or furan – 2 – acrylic acid, with 1 – tert-butoxycarbonyl piperazine generating amide reaction, the product in the presence of trifluoroacetic acid takes off uncle butoxycarbonyl, the obtained product with 2 – fluoro – 5 – [(4 – oxo – 3, 4 – […] – 1 – yl) methyl] benzoic acid generating amide reaction, to obtain a series of (E)- 4 – {3 – [4 – [(3 – substituted aromatic) acryloyl] piperazine – 1 – carbonyl] – 4 – fluorobenzyl} – 2 H – phthalazine – 1 – one derivatives. The initial pharmacological activity screening results show, the invention of the general formula of the compounds have certain in vitro PARP – 1 inhibition ability and the in vitro anti-tumor cell proliferation activity. The said compound of general structure is as follows: In the above formula: Ar selected from or R1 , R2 , R3 , R3 , R4 , R5 Can be a hydrogen atom, a fluorine atom, chlorine atom, bromine atom, methyl, methoxy, trifluoromethyl, nitro. (by machine translation)

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 763114-26-7

Reference£º
Phthalazine – Wikipedia,
Phthalazine | C8H6N754 – PubChem