N-(2-Fluoro-4-chloro-5-alkyloxyphenyl)-3,4-dimethyl-2-arylthio-5-oxo-2,5-dihydropyrrole 유도체 중 arylthio- 치환체들의 제초활성에 관한 구조-활성관계

Structure-activity relationships on the herbicidal activity of the arylthio substituents in N-(2-fluoro-4-chloro-5-alkyloxyphenyl)-3,4-dimethyl-2-arylthio-5-oxo-2,5-dihydropyrrole derivatives

  • 성낙도 (충남대학교 응용생물화학부) ;
  • 임치환 (충남대학교 응용생물화학부) ;
  • 윤기섭 (충남대학교 응용생물화학부) ;
  • 송종환 (한국화학연구소 신물질연구부) ;
  • 김형래 (한국화학연구소 신물질연구부)
  • Sung, Nack-Do (Department of Applied Biology and Chemistry, Chung-nam National University) ;
  • Lim, Chi-Whan (Department of Applied Biology and Chemistry, Chung-nam National University) ;
  • Yun, Ki-Seob (Department of Applied Biology and Chemistry, Chung-nam National University) ;
  • Song, Chong-Whan (Korea Research Institute Chemical Technology) ;
  • Kim, Hung-Rae (Korea Research Institute Chemical Technology)
  • 발행 : 2000.06.30

초록

N-(2-fluoro-4-chloro-5-alkyloxyphenyl)-3,4-dimethyl-2-arylthio-5-oxo-2,5-dihydro-pyrrole, 유도체들은 0.1 g/ha 이하의 농도에서 발아 후(Post-emergence), 벼와 논피 (Echinochloa crus-galli)와 올챙이고랭이 (Scriptus juncoides)에 대하여 선택성을 나타내었으며 pyrrole 고리상의 $SR_{2}$-기가 변화함에 따른 구조와 제초활성과의 관계 (SAR)를 청량적으로 검토하였다. 전체적으로 $R_{1}$=propargyl-치환체 (IA), $1{\sim}12$$R_{1}$=2-chloro-2-propenyl-치환체 (IB), $13{\sim}16$보다 높은 제초 활성을 나타내었으며 phenyl 고리상의 위치별 제초활성은 meta > para > ortho의 순으로 meta-치환체가 양호하였다. IA의 논피에 대한 제초활성은 $SR_{2}$-기가 Es상수의 적정값 $(Es)_{opt.}=3.25$을 가질 때 가장 큰 제초활성을 보인 반면에 올챙이 고랭이의 경우에는 MR상수에 의존적이었다.

A series of synthesized N-(2-fluoro-4-chloro-5-alkyloxyphenyl)-3,4-dimethyl-2-arylthio-5-oxo-2,5-dihydropyrrole derivatives as substrates were found to selectivity significantly with both rice plant (Oryza sativa L.) and weeds, barnyard grass (Echinochloa crus-galli) and bulrush (Scriptus juncoides) for those herbicidal activities at a rate of 0.1 kg/ha with post emergence under submerged conditions. The structure activity relationships (SARs) on herbicidal activity of $SR_{2}$=2-arylthio substituents on the pyrrole ring were analysized. From the results, the relative contribute orders of the $SR_{2}$ with phenyl group on the activity are meta > para > ortho-substituents. Among these compounds, the $R_{1}=propargyl$ (IA) subsrituents, $1{\sim}12$ showed higher activity than the $R_{1}$=2-chloro-2-propenyl (IB) substituents, $13{\sim}16$. The $SR_{2}$ groups of IA substituents shown that the optimal steric constant, $(Es)_{opt.}=3.25$ and m-phenylthio substituents were found to be -contribute the activity against barnyard grass. But the herbicidal activity of IB substituents against bulrush would depend upon the molar refractivity, $M_{R}$ constant of $SR_{2}$ group.

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