134962-85-9 + 134852-58-7 = 88255-01-0 反应条件:1.1 Solvents: Benzene 标题:New Process For Producing Phenylguanidine Derivatives 参考文献:Hungary
Ethanesulfonic Acid,2-[[[(Methoxycarbonyl)Amino][[2-Nitro-5-(Propylthio)Phenyl]Amino]Methylene]Amino]-,Monosodium Salt 反应生成 尼妥必敏 参考文献:Nafissi-Varchei,M. Mehdi 标题:Nafissi-Varchei,M. Mehdi
专利号:US-7893271-B2 优先权日:2005-07-28 标 题 :Benzimidazole carbamates and (thio) carbamates, and the synthesis and use thereof 发明人:CHASSAING CHRISTOPHE PIERRE ALAIN 权利人:INTERVET INT BV 摘要:This invention relates to benzimidazole carbamates and (thio)carbamates corresponding to Formula I: n nHere, X 1 and X 2 are independently O or S, wherein at least one of X 1 and X 2 is O; Y 1 and Y 2 are independently O or S, wherein at least one of Y 1 and Y 2 is O; R 1 is alkyl having from 1-4 carbon atoms; R 2 , R 3 , and R 4 are independently hydrogen or a cation; R 5 and R 6 are independently hydrogen, halogen, alkyl (having from 1-8 carbon atoms), —OR 7 , —SR 8 , —CO—R 9 , —OSO 2 —Ar, or —S(O)R 10 ; R 7 is alkyl having from 1-8 carbon atoms; R 8 is alkyl (having from 1-8 carbon atoms) or aryl; R 9 is alkyl (having from 1-8 carbon atoms), cycloalkyl (having from 3-6 carbon atoms), or aryl; Ar is aryl; and R 10 is alkyl (having from 1-8 carbon atoms) or aryl. The compounds generally are soluble and stable in water, and have antiparasitic (particularly anthelmintic) activity in vivo that is comparable to known water-insoluble benzimidazole carbamates (e.g., albendazole and fenbendazole).
专利号:ES-2344275-T3 优先权日:2005-07-28 标 题 :NEW (UNCLE) CARBAMATES FROM BENZIMIDAZOL WITH ANTIPARASITARY ACTIVITY AND SYNTHESIS OF THEM.
专利号:US-5278181-A 优先权日:1992-05-12 标 题 :Soluble alkyl[5-[amino (phenyl)methyl]-1H-benzimidazol-2-yl] carbamate anthelmintics 发明人:TOWNSEND LEROY B; WISE DEAN S; RAM SIYA 权利人:REGENTS ACTING ON BEHALF OF TH 摘要:Soluble alkyl (5-(amino (phenyl)methyl)-2H-benzimidazol-2-yl)carbamates, their enantiomorphic forms, and acid addition salts thereof are well absorbed and possess curative anthelmintic activity, especially against filarial worms, when administered orally or parenterally. Pharmaceutical compositions containing the compounds and methods of employing the compounds in methods of treating helminth infections in mammals are also disclosed, together with methods of synthesis.
专利号:CN-1191541-A 优先权日:1995-06-14 标题 :Synthesis modification of spinosyn compounds
专利号:PT-1913009-E 优先权日:2005-07-28 标 题 :NEW (TIO) CARBAMATES OF BENZIMIDAZOLE WITH ANTIPARASITARY ACTIVITY AND ITS SYNTHESIS
1. García-Llamazares JL, Alvarez-de-Felipe AI, Redondo-Cardeña P, Voces-Alonso JA, Prieto-Fernández JG. In vivo inhibition of the regenerative capacity of hydatid material after treatment with netobimin. Parasitol Res. 1997;83(2):105-8. doi: 10.1007/s004360050219. 86(3):514-20. doi: 10.1016/j.rvsc.2008.10.001. Epub 2008 Nov 20.
合成参考文献
参考文献:10.1007/bf03190008 摘要:Virkel G, Lifschitz A, Pis A, Lanusse C. Influence of diet on the pattern of gastrointestinal biotransformation of netobimin and albendazole sulphoxide in sheep. European Journal of Drug Metabolism and Pharmacokinetics. 1999 Mar;24(1):31–7. doi: 10.1007/bf03190008. 参考文献:10.1186/s12917-019-1968-8 摘要:Lambertz C, Poulopoulou I, Wuthijaree K, Gauly M. Anthelmintic efficacy against gastrointestinal nematodes in goats raised under mountain farming conditions in northern Italy. BMC Veterinary Research. 2019 Jun 27;15(1):216. doi: 10.1186/s12917-019-1968-8. 参考文献:10.1007/s004360050219 摘要:García-Llamazares JL, Alvarez-de-Felipe AI, Redondo-Cardeña P, Voces-Alonso JA, Prieto-Fernández JG. In vivo inhibition of the regenerative capacity of hydatid material after treatment with netobimin. Parasitol Res. 1997;83(2):105–8. doi: 10.1007/s004360050219. 参考文献:10.1186/1746-6148-6-8 摘要:Ceballos L, Moreno L, Alvarez L, Shaw L, Fairweather I, Lanusse C. Unchanged triclabendazole kinetics after co-administration with ivermectin and methimazole: failure of its therapeutic activity against triclabendazole-resistant liver flukes. BMC Veterinary Research. 2010 Feb 03;6(1):8. doi: 10.1186/1746-6148-6-8.