Synthesis of 2-amino-3-benzoylphenylacetic acid

2-Amino-3-benzoylphenylacetic acid, sodium salt was prepared from indoline through a process applicable to large scale production.     

Synthesis of 2-amino-3-fluoroacrylic acid containing peptides

[reaction: see text] Peptides containing (E)- and (Z)-3-fluorodehydroalanine have been prepared from serine via a fluoro-Pummerer rearrangement. The resulting electrophilic moieties may be useful affinity labels for the identification of the targets of dehydroamino acid containing natural products that act by covalent mechanisms.     

Synthesis and crystal structure of 4-amino-3-fluorophenylboronic acid

4-Amino-3-fluorophenyl boronic acid has been synthesized from 4-bromo-2-fluoroaniline by protecting the amine group and then carrying out a lithium-bromine exchange, followed by addition of trimethyl borate and then acidic hydrolysis. We obtained a 47% yield. We also measured the X-ray crystal structure. This derivative has a relatively low boronic acid pK_a value of 7.8 when acetylated or attached to acrylamide hydrogels. It also contains a pendant amine which facilitates attachment to polymers, for example. We are using this compound to construct glucose sensing materials that operates at the physiological pH of bodily fluids.     

Synthesis of 3-amino-4-nitropyrazoles

3-Bromo-1,5-dimethyl-4-nitropyrazole does not react upon heating with aqueous ammonia, while 1,5-dimethyl-3,4-dinitropyrazole under the same conditions yields 3-amino-1,5-dimethyl-4-nitropyrazole, which is formed from 3-bromo-1,5-dimethyl-4-nitropyrazole in the presence of a copper catalyst. The amination of 1-methyl-3,4-dinitropyrazole-5-carboxylic acid is accompanied by decarboxylation, which is characteristic for 4-substituted 1-methylpyrazole-5-carboxylic acids upon heating in aqueous ammonia or water.     

Synthesis of 2-amino-3-methoxypyrazinc

A new synthesis of 2-amiuo-3-methoxypyrazine, an intermediate in the synthesis of sulfalene, via 2-carbamido-3-hydroxy pyrazine and subsequent Hofmann rearrangement of 2-carhamido-3-methoxypyrazine, is described.     

Synthesis of some derivatives of 3-amino-3-desoxyerythrose and 3-amino-3-desoxy-D-3-erythrose

The synthesis of derivatives of 3-amino-3-deoxy-L-erythrose by LAH or LAD reduction of the oxime of 1,2-O-isopropylidene α-L -glycero-tetros-3-ulofuranose is described.     

Synthesis of 3-amino-4,5-dichloroisothiazole

4,5-Dichloro-1,2-thiazol-3-amine was synthesized starting from accessible 4,5-dichloro-1,2-thiazole-3-carbonyl azide and -3-carboxamide via Curtius and Hofmann rearrangements, respectively. The procedure involving Curtius rearrangement was found to be more advantageous from the preparative viewpoint.     

Synthesis of 3-amino-4-fluoropyrazoles

Fluorinated pyrazoles bearing additional functional groups that allow further functionalization are of considerable interest as building blocks in medicinal chemistry. The developed synthetic strategy for new 3-amino-4-fluoropyrazoles consists of a monofluorination of β-methylthio-β-enaminoketones using 1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor) toward the corresponding monofluorinated enaminoketones, followed by condensation with different hydrazines.     

Synthesis of 3-amino-5-nitrobenzaldehyde phenylhydrazone

Conclusions Conditions were found for the simultaneous reduction of the aliphatic nitro group and the selective reduction of one of the aromatic nitro groups in 3,5-dinitrophenylnitromethane and the previously unknown 3-amino-5-nitrobenzaldehyde was obtained as the phenylhydrazone.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2173–2175, September, 1982.     

Synthesis of substituted 2-amino-3-cyanopyrroles

A method was worked out for the preparation of substituted 2-amino-3-cyanopyrroles from N-acyl-α -amino ketones and malononitrile. Acyl derivatives of 2-amino-3-cyanopyrroles were obtained. A number of Mannich bases were synthesized by aminomethylation of 2-acetamido-3-cyano-4-phenylpyrrole.     

Synthesis of derivatives of 3-amino- and 3-aminomethylquinuclidine

Various methods of preparing 3-aminoquinuclidine from quinuclid-3-one oxime and hydrazone are developed. Quinuclidine derivatives with a substituted amino group at position 3 are synthesized.     

NitropyridineS. 9*. Synthesis of substituted 3-amino-5-nitropyridines

Substituted 3-amino-5-nitropyridines have been synthesized by the Curtius, Schmidt, and Hofmann reactions.     

Synthesis of derivatives of 4-amino-2-trifluoromethylnicotinic acid

The method for the synthesis of ethyl 4-R-amino-2-trifluoromethylnicotinates from a diphenylboron complex of ethyl 2-acetyl-3-amino-4,4,4-trifluorobut-2-enoate was developed.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2221–2223, October, 2004.     

Pyridazines. LIX. Synthesis of c-annelated pyridazines from 3-amino-4-pyridazinecarbonitrile

The utility of the aminonitrile 1 as an educt for the preparation of several new examples of heterocyclefused pyridazines (the [1,2,4]triazolo[1′,5′:1,6]pyrimido[4,5-c]pyridazine 7 , the pyrimido[4,5-c]pyridazines 8, 10a,b , and the pyrido[2,3-c]pyridazine 11 ) is demonstrated.     

Synthesis of derivatives of 2-amino-3-ethoxycarbonylthiophene

A number of alkylidene esters are synthesized from the corresponding ketones and cyanoacetic ester, and treatment of the esters with sulfur in the presence of a catalytic amount of diethylamine gives 2-amino-3-ethoxycarbonylthiophene derivatives.     

Synthesis of derivatives of 2-amino-3-ethoxycarbonylthiophene

A number of alkylidene esters are synthesized from the corresponding ketones and cyanoacetic ester, and treatment of the esters with sulfur in the presence of a catalytic amount of diethylamine gives 2-amino-3-ethoxycarbonylthiophene derivatives.