摘要:
The invention concerns a method for preparing a compound of formula (I) wherein: R1 represents a hydrogen or halogen atom or a C1-C4 alkyl group; R2, R3, R4, R5, R6, R7 represent each independently of one another a hydrogen or halogen atom or a C1-C4 alkyl, C1-C4 alkoxy, trifluoromethyl group; as well as their salts.
摘要:
The invention concerns a method for preparing a compound of formula (I) wherein: R1 represents a hydrogen or halogen atom or a C1-C4 alkyl group; R2, R3, R4, R5, R6, R7 represent each independently of one another a hydrogen or halogen atom or a C1-C4 alkyl, C1-C4 alkoxy, trifluoromethyl group; as well as their salts.
摘要:
The invention relates to a method of synthesis of ferroquine of formula (F) or of its metabolite of formula (Fm): comprising a reaction of reductive amination, said reaction comprising: (i) a stage of condensation of the aldhehyde-amino ferrocene of formula (1 ), which R represents a hydrogen atom or a methyl group, with the 7-chloroquinolin- amine of formula (2) as shown below, followed by (ii) a stage of reduction of the product of condensation obtained in the preceding stage (iii) then a stage of hydrolysis of the reaction mixture in the presence of an aqueous solution of ammonia or of citric acid.
摘要:
The invention relates to a method for preparing 3-keto-benzofurane derivatives of the general formula: Formula (I), where R is an alkyl or aryl group, R 1 is hydrogen or an alkyl or aryl group, and R 2 is a substituted alkyl or phenyl group. Said preparation method involves coupling a derivative of Formula III, where X is chlorine, bromine, or iodine or a sulfonate grouping: Formula (III) with a sulfonamide derivative of the formula R-SO 2 -NH 2 in the presence of a basic agent and a catalytic system formed of a complex between a palladium compound and a ligand.
摘要:
The present invention relates to ketobenzofuran derivatives of the general formula (D) shown below, as well as to a method for synthesising same by coupling a quinonimine and an enaminone by a Nenitzescu reaction and to the intermediates of the synthesis thereof.
摘要:
The invention relates a method for producing a compound of formula (I), wherein W is a -COOR group or CN radical, R1 is a hydrogen or halogen atom or a (Cl -C4)alkyl group, R3, R4, R5, R6, R7 represent independently of each other a hydrogen or halogen atom or a (Cl -C4)alkyl, (C1-C4)alkoxy or trifluoromethyl group and R is a (C1-C4)alkyl or benzyl group.
摘要:
The invention relates to a process for preparing benzofuran derivatives of general formula I, in which R represents a nitro or ester-COOR' group, where R' represents an alkyl group, R 1 represents hydrogen or an alkyl group and R 2 represents hydrogen, a halogen, a hydroxyl, haloalkyl, alkyl, alkoxy, dialkylaminoalkoxy or dialkylaminoalkyl group: by coupling the hydroxylamine with a diketone of general formula III: in order to form an oxime that is then cyclized by heating in order to form the desired compound.
摘要:
The invention relates to a process for preparing 5-aminobenzoylbenzofuran derivatives of formula (I), in which R 1 represents hydrogen or an alkyl group and R 2 represents hydrogen, an alkyl, alkoxy or dialkylaminoalkoxy group, by reduction of a 5-nitrobenzofuran derivative of formula (II) using a hydrogen transfer agent, in the presence of palladium-on-charcoal as catalyst and in an ether or an ether mixture as solvent.