Synthesis of Novel Pyrazolo[3,4-d][1,2,3]Triazines View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-07

AUTHORS

A. O. Gurenko, B. M. Khutova, S. V. Klyuchko, A. N. Vasilenko, V. S. Brovarets

ABSTRACT

Studies have been conducted of the reactions of 7-phenyl-3,7-dihydro-4H-pyrazolo[3,4-d]-[1,2,3]triazin-4-one with alkyl halides and formaldehyde, that occurred with retention of the pyrazolotriazine structure. Ethyl 2-(4-oxo-7-phenyl-4,7-dihydro-3H-pyrazolo[3,4-d][1,2,3]triazin-3-yl)-acetate was prepared by the reaction of 7-phenyl-3,7-dihydro-4H-pyrazolo[3,4-d][1,2,3]triazin-4-one with ethyl chloroacetate. It was used to synthesize the corresponding hydrazide with the aim of introducing the pyrazole or 1,3,4-oxadiazole fragments in the side chain of a bicyclic system. More... »

PAGES

528-536

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-014-1503-6

DOI

http://dx.doi.org/10.1007/s10593-014-1503-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1007426198


Indexing Status Check whether this publication has been indexed by Scopus and Web Of Science using the SN Indexing Status Tool
Incoming Citations Browse incoming citations for this publication using opencitations.net

JSON-LD is the canonical representation for SciGraph data.

TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

[
  {
    "@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
    "about": [
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0306", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Physical Chemistry (incl. Structural)", 
        "type": "DefinedTerm"
      }, 
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/03", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Chemical Sciences", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry", 
          "id": "https://www.grid.ac/institutes/grid.424920.9", 
          "name": [
            "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanska St., 02660, Kyiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Gurenko", 
        "givenName": "A. O.", 
        "id": "sg:person.014704175071.52", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014704175071.52"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry", 
          "id": "https://www.grid.ac/institutes/grid.424920.9", 
          "name": [
            "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanska St., 02660, Kyiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Khutova", 
        "givenName": "B. M.", 
        "id": "sg:person.016060743253.54", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016060743253.54"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry", 
          "id": "https://www.grid.ac/institutes/grid.424920.9", 
          "name": [
            "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanska St., 02660, Kyiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Klyuchko", 
        "givenName": "S. V.", 
        "id": "sg:person.015035075453.55", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015035075453.55"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry", 
          "id": "https://www.grid.ac/institutes/grid.424920.9", 
          "name": [
            "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanska St., 02660, Kyiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Vasilenko", 
        "givenName": "A. N.", 
        "id": "sg:person.016162601147.84", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016162601147.84"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry", 
          "id": "https://www.grid.ac/institutes/grid.424920.9", 
          "name": [
            "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanska St., 02660, Kyiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Brovarets", 
        "givenName": "V. S.", 
        "id": "sg:person.010072133553.61", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010072133553.61"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1007/s10593-012-1128-6", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1003281671", 
          "https://doi.org/10.1007/s10593-012-1128-6"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/hc.1024", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1008321616"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-013-1327-9", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1010511711", 
          "https://doi.org/10.1007/s10593-013-1327-9"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bcp.2006.03.006", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1011972072"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0223-5234(99)00126-9", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1015239822"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/ardp.19683011206", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1018039182"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/ardp.19683011206", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1018039182"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570230141", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1019078695"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570230141", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1019078695"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1080/15257770008032996", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1020367631"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570320502", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1022524046"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570320502", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1022524046"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0223-5234(01)01287-9", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1026581667"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/ardp.200700151", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1038399043"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jf801774k", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055925325"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jf801774k", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055925325"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm00373a020", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055945401"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo00932a009", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055991993"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2014-07", 
    "datePublishedReg": "2014-07-01", 
    "description": "Studies have been conducted of the reactions of 7-phenyl-3,7-dihydro-4H-pyrazolo[3,4-d]-[1,2,3]triazin-4-one with alkyl halides and formaldehyde, that occurred with retention of the pyrazolotriazine structure. Ethyl 2-(4-oxo-7-phenyl-4,7-dihydro-3H-pyrazolo[3,4-d][1,2,3]triazin-3-yl)-acetate was prepared by the reaction of 7-phenyl-3,7-dihydro-4H-pyrazolo[3,4-d][1,2,3]triazin-4-one with ethyl chloroacetate. It was used to synthesize the corresponding hydrazide with the aim of introducing the pyrazole or 1,3,4-oxadiazole fragments in the side chain of a bicyclic system.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s10593-014-1503-6", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1356886", 
        "issn": [
          "0009-3122", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "4", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "50"
      }
    ], 
    "name": "Synthesis of Novel Pyrazolo[3,4-d][1,2,3]Triazines", 
    "pagination": "528-536", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "235f6c42916066b344106b465998f3223f4425e5f8d79aee1e0e8907e9663097"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s10593-014-1503-6"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1007426198"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s10593-014-1503-6", 
      "https://app.dimensions.ai/details/publication/pub.1007426198"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-10T19:56", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-uberresearch-data-dimensions-target-20181106-alternative/cleanup/v134/2549eaecd7973599484d7c17b260dba0a4ecb94b/merge/v9/a6c9fde33151104705d4d7ff012ea9563521a3ce/jats-lookup/v90/0000000001_0000000264/records_8681_00000510.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007%2Fs10593-014-1503-6"
  }
]
 

Download the RDF metadata as:  json-ld nt turtle xml License info

HOW TO GET THIS DATA PROGRAMMATICALLY:

JSON-LD is a popular format for linked data which is fully compatible with JSON.

curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1007/s10593-014-1503-6'

N-Triples is a line-based linked data format ideal for batch operations.

curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/s10593-014-1503-6'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10593-014-1503-6'

RDF/XML is a standard XML format for linked data.

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10593-014-1503-6'


 

This table displays all metadata directly associated to this object as RDF triples.

133 TRIPLES      21 PREDICATES      41 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s10593-014-1503-6 schema:about anzsrc-for:03
2 anzsrc-for:0306
3 schema:author N3ea495bbe0b24f5fac9d9a808a22ac20
4 schema:citation sg:pub.10.1007/s10593-012-1128-6
5 sg:pub.10.1007/s10593-013-1327-9
6 https://doi.org/10.1002/ardp.19683011206
7 https://doi.org/10.1002/ardp.200700151
8 https://doi.org/10.1002/hc.1024
9 https://doi.org/10.1002/jhet.5570230141
10 https://doi.org/10.1002/jhet.5570320502
11 https://doi.org/10.1016/j.bcp.2006.03.006
12 https://doi.org/10.1016/s0223-5234(01)01287-9
13 https://doi.org/10.1016/s0223-5234(99)00126-9
14 https://doi.org/10.1021/jf801774k
15 https://doi.org/10.1021/jm00373a020
16 https://doi.org/10.1021/jo00932a009
17 https://doi.org/10.1080/15257770008032996
18 schema:datePublished 2014-07
19 schema:datePublishedReg 2014-07-01
20 schema:description Studies have been conducted of the reactions of 7-phenyl-3,7-dihydro-4H-pyrazolo[3,4-d]-[1,2,3]triazin-4-one with alkyl halides and formaldehyde, that occurred with retention of the pyrazolotriazine structure. Ethyl 2-(4-oxo-7-phenyl-4,7-dihydro-3H-pyrazolo[3,4-d][1,2,3]triazin-3-yl)-acetate was prepared by the reaction of 7-phenyl-3,7-dihydro-4H-pyrazolo[3,4-d][1,2,3]triazin-4-one with ethyl chloroacetate. It was used to synthesize the corresponding hydrazide with the aim of introducing the pyrazole or 1,3,4-oxadiazole fragments in the side chain of a bicyclic system.
21 schema:genre research_article
22 schema:inLanguage en
23 schema:isAccessibleForFree false
24 schema:isPartOf N73fd3aee5037409a91e3b25ae42c77c6
25 Nb269fc5a61254b93bf34475be01f4527
26 sg:journal.1356886
27 schema:name Synthesis of Novel Pyrazolo[3,4-d][1,2,3]Triazines
28 schema:pagination 528-536
29 schema:productId N34b67fbcf7674f8a9412b59d5e94f79b
30 N44585f0fabe94f9a9b31de26532dfa70
31 Nd83d694fc2e240ebbd2e8895ad6196b1
32 schema:sameAs https://app.dimensions.ai/details/publication/pub.1007426198
33 https://doi.org/10.1007/s10593-014-1503-6
34 schema:sdDatePublished 2019-04-10T19:56
35 schema:sdLicense https://scigraph.springernature.com/explorer/license/
36 schema:sdPublisher Na2040f85f97844a4b9d2cd75c86b04fb
37 schema:url http://link.springer.com/10.1007%2Fs10593-014-1503-6
38 sgo:license sg:explorer/license/
39 sgo:sdDataset articles
40 rdf:type schema:ScholarlyArticle
41 N3456cfbaee17427bb4aab238c885aa0e rdf:first sg:person.010072133553.61
42 rdf:rest rdf:nil
43 N34b67fbcf7674f8a9412b59d5e94f79b schema:name dimensions_id
44 schema:value pub.1007426198
45 rdf:type schema:PropertyValue
46 N3ea495bbe0b24f5fac9d9a808a22ac20 rdf:first sg:person.014704175071.52
47 rdf:rest Na6f4403cd61641e0b213385a7681ffcc
48 N44585f0fabe94f9a9b31de26532dfa70 schema:name readcube_id
49 schema:value 235f6c42916066b344106b465998f3223f4425e5f8d79aee1e0e8907e9663097
50 rdf:type schema:PropertyValue
51 N73fd3aee5037409a91e3b25ae42c77c6 schema:issueNumber 4
52 rdf:type schema:PublicationIssue
53 N791a44ff6ace4fb5828661f796b82f8c rdf:first sg:person.015035075453.55
54 rdf:rest Na44348c380ef4903a5c94624fb7b426f
55 Na2040f85f97844a4b9d2cd75c86b04fb schema:name Springer Nature - SN SciGraph project
56 rdf:type schema:Organization
57 Na44348c380ef4903a5c94624fb7b426f rdf:first sg:person.016162601147.84
58 rdf:rest N3456cfbaee17427bb4aab238c885aa0e
59 Na6f4403cd61641e0b213385a7681ffcc rdf:first sg:person.016060743253.54
60 rdf:rest N791a44ff6ace4fb5828661f796b82f8c
61 Nb269fc5a61254b93bf34475be01f4527 schema:volumeNumber 50
62 rdf:type schema:PublicationVolume
63 Nd83d694fc2e240ebbd2e8895ad6196b1 schema:name doi
64 schema:value 10.1007/s10593-014-1503-6
65 rdf:type schema:PropertyValue
66 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
67 schema:name Chemical Sciences
68 rdf:type schema:DefinedTerm
69 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
70 schema:name Physical Chemistry (incl. Structural)
71 rdf:type schema:DefinedTerm
72 sg:journal.1356886 schema:issn 0009-3122
73 1573-8353
74 schema:name Chemistry of Heterocyclic Compounds
75 rdf:type schema:Periodical
76 sg:person.010072133553.61 schema:affiliation https://www.grid.ac/institutes/grid.424920.9
77 schema:familyName Brovarets
78 schema:givenName V. S.
79 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010072133553.61
80 rdf:type schema:Person
81 sg:person.014704175071.52 schema:affiliation https://www.grid.ac/institutes/grid.424920.9
82 schema:familyName Gurenko
83 schema:givenName A. O.
84 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014704175071.52
85 rdf:type schema:Person
86 sg:person.015035075453.55 schema:affiliation https://www.grid.ac/institutes/grid.424920.9
87 schema:familyName Klyuchko
88 schema:givenName S. V.
89 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015035075453.55
90 rdf:type schema:Person
91 sg:person.016060743253.54 schema:affiliation https://www.grid.ac/institutes/grid.424920.9
92 schema:familyName Khutova
93 schema:givenName B. M.
94 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016060743253.54
95 rdf:type schema:Person
96 sg:person.016162601147.84 schema:affiliation https://www.grid.ac/institutes/grid.424920.9
97 schema:familyName Vasilenko
98 schema:givenName A. N.
99 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016162601147.84
100 rdf:type schema:Person
101 sg:pub.10.1007/s10593-012-1128-6 schema:sameAs https://app.dimensions.ai/details/publication/pub.1003281671
102 https://doi.org/10.1007/s10593-012-1128-6
103 rdf:type schema:CreativeWork
104 sg:pub.10.1007/s10593-013-1327-9 schema:sameAs https://app.dimensions.ai/details/publication/pub.1010511711
105 https://doi.org/10.1007/s10593-013-1327-9
106 rdf:type schema:CreativeWork
107 https://doi.org/10.1002/ardp.19683011206 schema:sameAs https://app.dimensions.ai/details/publication/pub.1018039182
108 rdf:type schema:CreativeWork
109 https://doi.org/10.1002/ardp.200700151 schema:sameAs https://app.dimensions.ai/details/publication/pub.1038399043
110 rdf:type schema:CreativeWork
111 https://doi.org/10.1002/hc.1024 schema:sameAs https://app.dimensions.ai/details/publication/pub.1008321616
112 rdf:type schema:CreativeWork
113 https://doi.org/10.1002/jhet.5570230141 schema:sameAs https://app.dimensions.ai/details/publication/pub.1019078695
114 rdf:type schema:CreativeWork
115 https://doi.org/10.1002/jhet.5570320502 schema:sameAs https://app.dimensions.ai/details/publication/pub.1022524046
116 rdf:type schema:CreativeWork
117 https://doi.org/10.1016/j.bcp.2006.03.006 schema:sameAs https://app.dimensions.ai/details/publication/pub.1011972072
118 rdf:type schema:CreativeWork
119 https://doi.org/10.1016/s0223-5234(01)01287-9 schema:sameAs https://app.dimensions.ai/details/publication/pub.1026581667
120 rdf:type schema:CreativeWork
121 https://doi.org/10.1016/s0223-5234(99)00126-9 schema:sameAs https://app.dimensions.ai/details/publication/pub.1015239822
122 rdf:type schema:CreativeWork
123 https://doi.org/10.1021/jf801774k schema:sameAs https://app.dimensions.ai/details/publication/pub.1055925325
124 rdf:type schema:CreativeWork
125 https://doi.org/10.1021/jm00373a020 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055945401
126 rdf:type schema:CreativeWork
127 https://doi.org/10.1021/jo00932a009 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055991993
128 rdf:type schema:CreativeWork
129 https://doi.org/10.1080/15257770008032996 schema:sameAs https://app.dimensions.ai/details/publication/pub.1020367631
130 rdf:type schema:CreativeWork
131 https://www.grid.ac/institutes/grid.424920.9 schema:alternateName Institute of Bioorganic Chemistry and Petrochemistry
132 schema:name Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanska St., 02660, Kyiv, Ukraine
133 rdf:type schema:Organization
 




Preview window. Press ESC to close (or click here)


...