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Pyrimidinyl‐substituted amides and thioureas: syntheses, crystal structure and herbicidal activities
Author(s) -
Liu GuoHua,
Xue YunNing,
Lu XiaoQuan,
Liu MouMing,
Wang WeiYing,
Yang LiangZhun
Publication year - 2008
Publication title -
pest management science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.296
H-Index - 125
eISSN - 1526-4998
pISSN - 1526-498X
DOI - 10.1002/ps.1509
Subject(s) - digitaria sanguinalis , pyrimidine , echinochloa , brassica , digitaria , chemistry , sorghum , ring (chemistry) , stereochemistry , organic chemistry , biology , weed , botany , agronomy
BACKGROUND: The high herbicidal activities of [1,2,4]triazolo[1,5‐ c ]pyrimidine and 2H ‐1,2,4‐thiadiazolo[2,3‐ a ]pyrimidine derivatives suggested the development of new fused heterocyclic compounds for application as herbicides. RESULTS: Three series of pyrimidinyl‐substituted thioureas (4) and amides (5, 6) were synthesized, and the typical crystal structure of a 2H ‐1,2,4‐thiadiazolo[2,3‐ a ]pyrimidine derivative (5a) was determined by X‐ray diffraction. All the compounds were tested for herbicidal activity against selected weeds. CONCLUSION: The series of fused heterocyclic amides 5a to 5d exhibited high herbicidal activities both against monocotyledonous weeds ( Echinochloa crus‐galli L., Sorghum bicolor (L.) Mönch., Digitaria sanguinalis (L.) Scop) and against dicotyledonous weeds ( Amaranthus retroflexus L. and Brassica campestris L.) in pre‐emergence treatments. In particular, compound 5b at low concentration still showed high inhibitory activity against A. retroflexus in pre‐emergence treatment. Different substituents at the meta positions of the pyrimidine ring were found to affect the herbicidal activity. Copyright © 2007 Society of Chemical Industry