제초성 Benzenesulfonyl urea계 화합물의 형태와 반응성

Conformation and Reactivity of Herbicidal Benzenesulfonyl urea Compounds

제초성 비치환(H) benzenesulfonyl urea 분자, 1은 sulfonyl group 인접의 amino group과 pyrimidinyl group의 N원자 사이에 회합(H-결합)된 형태(II-keto)가 제일 안정하였으며 phenyl 치환$(R_2$ 및 $R_3)$유도체, 2는 전자를 밀수록$(\sigma<0)$ LUMO(ev.)는 음의 값으로 증가하여 물 분자의 HOMO(ev.)사이에 궤도 조절반응(p<0)에따른 전형적인 친핵 반응성을 나타낸다. N-(4,6-이치환-pyrimidine-2-yl)aminocarbonyl-2-(1,1-dimethoxy-2-fluoro)ethylbenzenesulfonamides, 3 및 N-(4,6-이치환-triazine-2-yl)aminocarbonyl-2-(1,1-dimethoxy-2-리uoro)ethylbenzenesulfonamide, 4 유도체의 4,6-이치환기(X 및 Y) 와 헤테로 고리의 변화에 따른 올챙이고랭이(Scirpus juncodies.) 에 대한 제초활성은 소수성$((log\;P)_{opt.}=0.89)$이 가장 큰 영향을 미치는 요인이었다. 또한, pyrimidine-치환체, 3이 triazine-치환체, 4보다 양호한 제초활성을 나타내었으며 dimethoxypyrimidine-치환체, 3a가 가장 큰 제초활성을 보였다.

The most stable stereo conformer in non substituted benzenesulfonyl urea, 1 was the II-keto form, which the molecule was intramolecular associated(H-bond) coformer between imide group and N atom on the Pyrimidine ring. The hydrolytic degradation of 2 derivatives were proceeds by nucleophilic addition reaction(p<0) with orbital controlled intermolecular interaction between LUMO with electron donating$(\sigma<0)$ groups of 2 and HOMO of water molecule. N-(4,6-disub. pyrimid ine-2-yl)aminocarbonyl-2-(1,1-dimethoxy-2-fluoro)ethylbenze nesulfonamides,3 and N-(4,6-disub. triazine-2-yl)aminocarbonyl-2-(1,1-d imethoxy-2-fluoro)ethylbenzenesulfonamides,4 we re synthesized and their herbicidal activities in vivo against bulrush (Scirpus juncoides.) were measured by the pot test under the paddy conditions And the structure activity relationships(SAR) were analyzed by the multiple regression technique. The results of the SAR suggested that the 3 and 4 derivatives indicated dependent on the hydrophobicity of the 4,6-disubstituents and the heterocyclo group, where the optimal value $((log\;P)_{opt.}=0.89)$ of hydrophobicity was 0.89. The pyrimidine substituents, 3 showed higher herbicidal activity than the triazine substituents, 4. Among them, 4,6-dimethoxypyrimidine substituent, 3a showed the best herbicidal activity.