STUDIES ON THE ALKYLATION OF QUINOLIN-2(1H)-ONE DERIVATIVES

Alkylation of quinolin-2(1H)-one (1) and its C(6) and C(7) substituted dervatives (OMe, OBn, and Cl) with 2-bromoacetophenone or chloroacetone under basic condition (K2CO3 in DMF) gave a mixture of N1- and O2- alkylated products with the former one as a major product. However, alkylation of 8-methox...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: CHEN,CHIA-LING, CHEN,I-LI, CHEN,JIH-JUNG, WEI,DAU-CHANG, HSIEH,HAN-JIE, CHANG,KEN-MING, TZENG,CHERNG-CHYI, WANG,TAI-CHI
Lenguaje:English
Publicado: Sociedad Chilena de Química 2015
Materias:
Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072015000100008
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:scielo:S0717-97072015000100008
record_format dspace
spelling oai:scielo:S0717-970720150001000082015-04-21STUDIES ON THE ALKYLATION OF QUINOLIN-2(1H)-ONE DERIVATIVESCHEN,CHIA-LINGCHEN,I-LICHEN,JIH-JUNGWEI,DAU-CHANGHSIEH,HAN-JIECHANG,KEN-MINGTZENG,CHERNG-CHYIWANG,TAI-CHI N-Alkylation O-Alkylation Quinolin-2(1H)-one Alkylation of quinolin-2(1H)-one (1) and its C(6) and C(7) substituted dervatives (OMe, OBn, and Cl) with 2-bromoacetophenone or chloroacetone under basic condition (K2CO3 in DMF) gave a mixture of N1- and O2- alkylated products with the former one as a major product. However, alkylation of 8-methoxy-, 8-benzyloxy-, and 8-chloro- quinolin-2(1H)-ones under the same reaction conditions gave exclusively O2-alkylated products.info:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.60 n.1 20152015-03-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072015000100008en10.4067/S0717-97072015000100008
institution Scielo Chile
collection Scielo Chile
language English
topic N-Alkylation
O-Alkylation
Quinolin-2(1H)-one
spellingShingle N-Alkylation
O-Alkylation
Quinolin-2(1H)-one
CHEN,CHIA-LING
CHEN,I-LI
CHEN,JIH-JUNG
WEI,DAU-CHANG
HSIEH,HAN-JIE
CHANG,KEN-MING
TZENG,CHERNG-CHYI
WANG,TAI-CHI
STUDIES ON THE ALKYLATION OF QUINOLIN-2(1H)-ONE DERIVATIVES
description Alkylation of quinolin-2(1H)-one (1) and its C(6) and C(7) substituted dervatives (OMe, OBn, and Cl) with 2-bromoacetophenone or chloroacetone under basic condition (K2CO3 in DMF) gave a mixture of N1- and O2- alkylated products with the former one as a major product. However, alkylation of 8-methoxy-, 8-benzyloxy-, and 8-chloro- quinolin-2(1H)-ones under the same reaction conditions gave exclusively O2-alkylated products.
author CHEN,CHIA-LING
CHEN,I-LI
CHEN,JIH-JUNG
WEI,DAU-CHANG
HSIEH,HAN-JIE
CHANG,KEN-MING
TZENG,CHERNG-CHYI
WANG,TAI-CHI
author_facet CHEN,CHIA-LING
CHEN,I-LI
CHEN,JIH-JUNG
WEI,DAU-CHANG
HSIEH,HAN-JIE
CHANG,KEN-MING
TZENG,CHERNG-CHYI
WANG,TAI-CHI
author_sort CHEN,CHIA-LING
title STUDIES ON THE ALKYLATION OF QUINOLIN-2(1H)-ONE DERIVATIVES
title_short STUDIES ON THE ALKYLATION OF QUINOLIN-2(1H)-ONE DERIVATIVES
title_full STUDIES ON THE ALKYLATION OF QUINOLIN-2(1H)-ONE DERIVATIVES
title_fullStr STUDIES ON THE ALKYLATION OF QUINOLIN-2(1H)-ONE DERIVATIVES
title_full_unstemmed STUDIES ON THE ALKYLATION OF QUINOLIN-2(1H)-ONE DERIVATIVES
title_sort studies on the alkylation of quinolin-2(1h)-one derivatives
publisher Sociedad Chilena de Química
publishDate 2015
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072015000100008
work_keys_str_mv AT chenchialing studiesonthealkylationofquinolin21honederivatives
AT chenili studiesonthealkylationofquinolin21honederivatives
AT chenjihjung studiesonthealkylationofquinolin21honederivatives
AT weidauchang studiesonthealkylationofquinolin21honederivatives
AT hsiehhanjie studiesonthealkylationofquinolin21honederivatives
AT changkenming studiesonthealkylationofquinolin21honederivatives
AT tzengcherngchyi studiesonthealkylationofquinolin21honederivatives
AT wangtaichi studiesonthealkylationofquinolin21honederivatives
_version_ 1718445530625867776