Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Guanidines, formation

Preparing to install the A and B rings, 34 was converted to isourea 35, remarkably without erosion of the C7 stereochemistry. The missing part was introduced with Grignard compound 36, and after oxidation and O-deprotection the two final rings were closed via guanidine formation with buffered ammonia (20 % overall) to yield penta-cycle 37. [Pg.243]

The RNAse model compound of Hamilton was constructed in a few steps (Scheme 15) [30]. Benzoyl isothiocyanate was allowed to react with diamine 59 to yield bis(thiourea) 61 after deprotection. S-methylation activated the urea moieties for guanidine formation with Af,A -dimethyl-ethy-lenediamine 62 to reach the desired compound 53. [Pg.248]

Treatment of 8-azidomethylperhydropyrido[l,2-c]pyrimidin-l-one 157 with methyl triflate and catalytic hydrogenation of the azide group led to the formation of tricyclic guanidine derivative 158 (01JA8851). Hydroxy group of 149 was protected with methoxymethyl chloride, and the p-methoxybenzyl protecting group (PMB) was eliminated by treatment with DDQ. [Pg.254]

Interposition of a methylene group between the phenyl ring and the heterocycle leads to the benzyldiami nopyrimidines, a class of compounds notable for their antibacterial activity. Condensation of hydrocinnamate 54 with ethyl formate leads to the hydroxymethylene derivative 55. In this case, too, the heterocyclic ring is formed by reaction with guanidine. This sequence probably involves initial addition-elimination to the forniyl carbon to form 56 cyclization in this case involves simple amide formation. Tautomerization then affords the hydroxy derivative 57. This is converted to tetroxoprim (58) by first... [Pg.154]

One such compound, bropirimine (112), is described as an agent which has both antineo-plastic and antiviral activity. The first step in the preparation involves formation of the dianion 108 from the half ester of malonic acid by treatment with butyllithium. Acylation of the anion with benzoyl chloride proceeds at the more nucleophilic carbon anion to give 109. This tricarbonyl compound decarboxylates on acidification to give the beta ketoester 110. Condensation with guanidine leads to the pyrimidone 111. Bromination with N-bromosuccinimide gives bropirimine (112) [24]. [Pg.117]

Reaction of 2,3-dichlorobenzoyl chloride with cyanide ion leads to the corresponding benzoyl cyanide (141). Condensation of that reactive intermediate with aminoguanidine 142 leads to the hydrazone-like product 143. Treatment with base results in addition of one of the guanidine amino groups to the nitrile function and formation of the 1,2,4-triazine ring. The product, lamo-trigine (144), is described as an anticonvulsant agent [31]. [Pg.120]

A useful route to 2,1,3-benzothiadiazoles is the F -catalyzed cyclization of l-(4-X-C6F4)-3-trimethylsilyl-l, 3-diaza-2-thiallenes [90JFC(50)359]. Fluoride ion catalysis is also used in the formation of heterocycles from pentafluorobenzoyl and -phenoxy compounds (81BCJ3447). Pentafluoro-phenylcarbonimidoyl dichloride with primary amines gave guanidines,... [Pg.13]

Especially notable is also the synthesis and structural characterization of an unusual antimony(III) guanidinate. 1,2,3-Tiiisopropylguanidine, Pr N = C(NHPr )2,was found to react with 1 molar equivalent of Sb(NMe2)3 in toluene under formation of a yellow solution, from which the novel compound Sb[Pr NC(NPr )2][Pr NHC(NPr )2] could be isolated in 10% yield as highly air-sensitive crystals. In the solid state, the complex adopts a heavily distorted trigonal-bipyramidal molecular structure in which the Sb is chelated by a [CfNPr ls] dianion and a [Pr NHC(NPr )2] monoanion (Figure 16). Supramolecular... [Pg.225]

Metathetical routes using bulky lithium guanidinates as starting materials have also been employed to synthesize bis(guanidinato) lanthanide halides as well as reactive alkyls and hydrides. Scheme 63 shows as a typical example the formation of the lutetium chloro precursor, which was isolated in 76% yield. ... [Pg.231]

Homoleptic lanthanide(III) tris(amidinates) and guanidinates are among the longest known lanthanide complexes containing these chelating ligands. In this area the carbodiimide insertion route is usually not applicable, as simple, well-defined lanthanide tris(alkyls) and tris(dialkylamides) are not readily available. A notable exception is the formation of homoleptic lanthanide guanidinates from... [Pg.234]

The formation of a bis(guanidinate)-supported titanium imido complex has been achieved in different ways, two of which are illustrated in Scheme 90. The product is an effective catalyst for the hydroamination of alkynes (cf. Section V.B). It also undergoes clean exchange reactions with other aromatic amines to afford new imide complexes such as [Me2NC(NPr )2]2Ti = NC6F5. ... [Pg.252]

Unique examples of N,A/ , N "-tri(isopropyl)guanidinate complexes of Nb(V) and Ta(V) bearing additional terminal imido ligands have been obtained as depicted in Scheme 116. Depending on the reaction conditions, these reactions may also lead to the formation of compounds containing dianionic guanidinate... [Pg.265]

AnUine, however, is too toxic for use in mbber products. Its less toxic reaction product with carbondisulfide, thiocarbanihde, was introduced as an accelerator in 1907. Further developments led to guanidine accelerator [4]. Reaction products formed between carbon disulfide and aliphatic amines (dithiocarbamates) were first used as accelerators in 1919 [5]. These were and still are the most active accelerators in respect to both cross-finking rates and extent of cross-link formation. However, most dithiocarbamates accelerators give little or no scorch resistance and therefore cannot be used in aU applications. [Pg.416]


See other pages where Guanidines, formation is mentioned: [Pg.320]    [Pg.554]    [Pg.41]    [Pg.656]    [Pg.554]    [Pg.247]    [Pg.41]    [Pg.57]    [Pg.554]    [Pg.450]    [Pg.469]    [Pg.3]    [Pg.3]    [Pg.148]    [Pg.148]    [Pg.320]    [Pg.554]    [Pg.41]    [Pg.656]    [Pg.554]    [Pg.247]    [Pg.41]    [Pg.57]    [Pg.554]    [Pg.450]    [Pg.469]    [Pg.3]    [Pg.3]    [Pg.148]    [Pg.148]    [Pg.303]    [Pg.113]    [Pg.114]    [Pg.130]    [Pg.2059]    [Pg.1057]    [Pg.179]    [Pg.222]    [Pg.262]    [Pg.263]    [Pg.278]    [Pg.153]    [Pg.113]    [Pg.83]    [Pg.182]    [Pg.187]    [Pg.222]    [Pg.229]    [Pg.275]    [Pg.290]    [Pg.336]   
See also in sourсe #XX -- [ Pg.59 , Pg.528 ]




SEARCH



Pyrimidine formation guanidine

Reaction CXXX.—Formation of Amino Guanidine Derivatives

© 2024 chempedia.info