Synthesis of new potential active homodrimane sesquiterpenoids with 1,3,4-thiadiazole units
Închide
Articolul precedent
Articolul urmator
858 6
Ultima descărcare din IBN:
2023-06-30 10:42
SM ISO690:2012
LUNGU, Lidia, CIOCARLAN, Alexandru, ARICU, Aculina, ILKER, Ozer, BARBA, Alic. Synthesis of new potential active homodrimane sesquiterpenoids with 1,3,4-thiadiazole units. In: Achievements and perspectives of modern chemistry, 9-11 octombrie 2019, Chişinău. Chisinau, Republic of Moldova: Tipografia Academiei de Ştiinţe a Moldovei, 2019, p. 225. ISBN 978-9975-62-428-2.
EXPORT metadate:
Google Scholar
Crossref
CERIF

DataCite
Dublin Core
Achievements and perspectives of modern chemistry 2019
Conferința "International Conference "Achievements and perspectives of modern chemistry""
Chişinău, Moldova, 9-11 octombrie 2019

Synthesis of new potential active homodrimane sesquiterpenoids with 1,3,4-thiadiazole units


Pag. 225-225

Lungu Lidia, Ciocarlan Alexandru, Aricu Aculina, Ilker Ozer, Barba Alic
 
Institute of Chemistry
 
 
Disponibil în IBN: 11 noiembrie 2019


Rezumat

Sesquiterpenoids, especially those with a homodrimane skeleton, are natural compounds with a wide range of pharmaceutical and biological activities [1]. The 1,3,4-thiadiazole and its derivatives are considered interesting heterocycles since they possess important pharmacological activities [2]. As starting material for the synthesis of new title compounds 11-homodrim-6,8-dien-12-oic acid 2 was used. It was obtained before from commercially available sclareolide 1in 5 steps, with an overall yield of 47%, as depicted in Scheme [3]. After that coupling reaction of acid 2 with hydrazine hydrate was performed. Subsequently, was used one-pot method, that includes the interaction of the hydrazide 3 with a series of substituted isothiocyanates, without isolation of the intermediate compounds. This reaction was carried out in the presence of triethylamine (Et3N) in water, giving desired homodrimane compounds bearing 1,3,4-thiadiazole units in 72-78% yields [4].formulaReagents: a. NH2-NH2·H2O, EtOH, delta, 5h, 85%; b. R-NCS, Et3N, H2O, delta, 18h, 72-78%. Scheme.Thesynthesis of homodrimane sesquiterpenoids with 1,3,4-thiadiazole units. The structures of compounds 4a-c were fully confirmed based on their 1H, 13C, 15N and 2D NMR data.

Cerif XML Export

<?xml version='1.0' encoding='utf-8'?>
<CERIF xmlns='urn:xmlns:org:eurocris:cerif-1.5-1' xsi:schemaLocation='urn:xmlns:org:eurocris:cerif-1.5-1 http://www.eurocris.org/Uploads/Web%20pages/CERIF-1.5/CERIF_1.5_1.xsd' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' release='1.5' date='2012-10-07' sourceDatabase='Output Profile'>
<cfResPubl>
<cfResPublId>ibn-ResPubl-87373</cfResPublId>
<cfResPublDate>2019</cfResPublDate>
<cfStartPage>225</cfStartPage>
<cfISBN>978-9975-62-428-2</cfISBN>
<cfURI>https://ibn.idsi.md/ro/vizualizare_articol/87373</cfURI>
<cfTitle cfLangCode='EN' cfTrans='o'>Synthesis of new potential active homodrimane sesquiterpenoids with 1,3,4-thiadiazole units</cfTitle>
<cfAbstr cfLangCode='EN' cfTrans='o'><p>Sesquiterpenoids, especially those with a homodrimane skeleton, are natural compounds with a wide range of pharmaceutical and biological activities [1]. The 1,3,4-thiadiazole and its derivatives are considered interesting heterocycles since they possess important pharmacological activities [2]. As starting material for the synthesis of new title compounds 11-homodrim-6,8-dien-12-oic acid 2 was used. It was obtained before from commercially available sclareolide 1in 5 steps, with an overall yield of 47%, as depicted in Scheme [3]. After that coupling reaction of acid 2 with hydrazine hydrate was performed. Subsequently, was used one-pot method, that includes the interaction of the hydrazide 3 with a series of substituted isothiocyanates, without isolation of the intermediate compounds. This reaction was carried out in the presence of triethylamine (Et3N) in water, giving desired homodrimane compounds bearing 1,3,4-thiadiazole units in 72-78% yields [4].</p><p>formula</p><p>Reagents: a. NH2-NH2&middot;H2O, EtOH, delta, 5h, 85%; b. R-NCS, Et3N, H2O, delta, 18h, 72-78%. Scheme.Thesynthesis of homodrimane sesquiterpenoids with 1,3,4-thiadiazole units. The structures of compounds 4a-c were fully confirmed based on their 1H, 13C, 15N and 2D NMR data.</p></cfAbstr>
<cfResPubl_Class>
<cfClassId>eda2d9e9-34c5-11e1-b86c-0800200c9a66</cfClassId>
<cfClassSchemeId>759af938-34ae-11e1-b86c-0800200c9a66</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
</cfResPubl_Class>
<cfResPubl_Class>
<cfClassId>e601872f-4b7e-4d88-929f-7df027b226c9</cfClassId>
<cfClassSchemeId>40e90e2f-446d-460a-98e5-5dce57550c48</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
</cfResPubl_Class>
<cfPers_ResPubl>
<cfPersId>ibn-person-23821</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-12404</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-11130</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-58399</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-11134</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
</cfPers_ResPubl>
</cfResPubl>
<cfPers>
<cfPersId>ibn-Pers-23821</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-23821-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
<cfFamilyNames>Lungu</cfFamilyNames>
<cfFirstNames>Lidia</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-12404</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-12404-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
<cfFamilyNames>Ciocarlan</cfFamilyNames>
<cfFirstNames>Alexandru</cfFirstNames>
<cfFamilyNames>Чекырлан</cfFamilyNames>
<cfFirstNames>А.</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-11130</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-11130-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
<cfFamilyNames>Aricu</cfFamilyNames>
<cfFirstNames>Aculina</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-58399</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-58399-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
<cfFamilyNames>Ilker</cfFamilyNames>
<cfFirstNames>Ozer</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-11134</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-11134-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2019T24:00:00</cfStartDate>
<cfFamilyNames>Barba</cfFamilyNames>
<cfFirstNames>Alic</cfFirstNames>
<cfFamilyNames>Барба</cfFamilyNames>
<cfFirstNames>Алик</cfFirstNames>
</cfPersName_Pers>
</cfPers>
</CERIF>