1,2,4-Triazole

O=C(CC(F)=C(F)F)n1cncn1
Reaction #1044
desired product
Выход 94.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #4220
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1yl)butan-2-ol
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)C(O)(C=Cc1ccc(Cl)cc1)Cn1ccnc1
Reaction #4222
1-(4-chlorophenyl)-4,4-dimethyl-3-(imidazol-1-yl-methyl)-1-penten-3-ol
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)C(O)(CCc1ccc(Cl)cc1)Cn1cncn1
Reaction #4223
1-(4-chlorophenyl)-4,4-dimethyl-3-(1,2,4-triazol-1-yl-methyl)-pentane-3-ol
Выход 53.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
FC(F)(F)C(F)(F)C(F)(F)C1(Cn2cncn2)CO1
Reaction #4819
2-heptafluoropropyl-2-(1H-1,2,4-triazol-1-ylmethyl)oxirane
Выход 2.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1cc(-c2nc3ccccc3o2)ccc1Cn1cncn1
Reaction #7838
2-[3-methoxy-4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(Cn1cncn1)Cn1cncn1
Reaction #10856
1,3-bis(1,2,4-triazole-1-yl)-propan-2-on
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc(C(c2ccccc2)(c2ccccc2)n2cncn2)cc1
Reaction #11327
1-trityl-1H-1,2,4-triazole
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C([O-])c1nc[nH]n1.[Na+]
Reaction #11834
sodium 1,2–4-triazolate
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cn1ncc(C(=O)NC2C3CC4CC(C3)CC2C4)c1-n1cncn1
Reaction #41117
Methyl-5-[1,2,4]triazol-1-yl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Oc2cc(Oc3cccnc3)cc3[nH]c(-n4cncn4)nc23)cc1
Reaction #41532
4-(4-fluoro-phenoxy)-6-(pyridin-3-yloxy)-2-[1,2,4]triazol-1-yl-1H-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ncnn2c(C3CCC3)nc(-c3cccc(OCc4ccccc4)c3)c12
Reaction #46250
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1OCCCCCn1cncn1
Reaction #48996
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)OC(=O)c2ccc(C(c3c(F)cc([N+](=O)[O-])cc3F)n3cncn3)cc21
Reaction #50336
5-[(2,6-difluoro- 4-nitrophenyl)-[1,2,4]triazol-1-yl-methyl]-3,3-dimethyl-3H-isobenzofuran-1-one
Выход 67.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(c1ccccc1)C(C(=O)c1ccccc1)n1cncn1
Reaction #54238
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=C(Cn1cncn1)c1ccc(Cl)cc1
Reaction #54239
2-(1,2,4-triazol-1-yl)-4'-chloroacetophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCC(Oc1cc(Cl)cc(Cl)c1)C(=O)NC(C)(C)C#CCCCn1cncn1
Reaction #57503
required product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CS(=O)(=O)c1ccc(-n2cncn2)c(C(=O)N2CCN(c3ccc(C(F)(F)F)cc3)CC2)c1
Reaction #61046
title compound
Выход 6.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cc(C)nc(NCn2cncn2)n1
Reaction #63144
4-methoxy-6-methyl-2-(1,2,4-triazol-1-ylmethylamino)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
c1ccc2ncncc2c1
Reaction #64113
Quinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
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