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213514

CC(=O)NNC(=O)c1c(-c2c(F)cccc2Cl)noc1-c1cnn(-c2ccccc2F)c1C(F)(F)F
Reaction #301262
DOI: 10.1039/C8SC04228D
Cc1onc(-c2ccccc2)c1C(=O)NN
Reaction #1288049
DOI: 10.1039/C8SC04228D
Cc1onc(-c2ccccc2)c1-c1nnc2n1Cc1ccc(I)cc1-2
Reaction #1881460
8-iodo-3-(5-methyl-3-phenylisoxazol-4-yl)-5H-[1,2,4]-triazolo[3,4-a]isoindole
Ausbeute 57.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NNC(=O)c2c(-c3ccccc3)noc2C)cc1
Reaction #1881471
title compound
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NNC(=O)c2c(-c3ccccc3)noc2C)cc1
Reaction #1881472
title compound
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(-c2c(-c3c(F)cccc3Cl)noc2-c2cnn(-c3ccncc3)c2C(F)(F)F)s1
Reaction #1892444
3-(2-chloro-6-fluorophenyl)-4-(5-methyl-1,3,4-thiadiazol-2-yl)-5-(1-(pyridin-4-yl)-5-(trifluoromethyl)-1H-pyrazol-4-yl)isoxazole
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccccc1-n1ncc(-c2onc(-c3c(F)cccc3Cl)c2-c2nnco2)c1C(F)(F)F
Reaction #1892445
yellowish solid
Ausbeute 46.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NNC(=O)c1c(-c2c(F)cccc2Cl)noc1-c1cnn(-c2ccccc2F)c1C(F)(F)F
Reaction #1892459
compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1C(=O)NN
Reaction #2070262
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1-c1nnc(-c2ccccc2)o1
Reaction #2070263
title compound
Ausbeute 58.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1nnc(-c2c(-c3ccccc3)noc2C)o1
Reaction #2070264
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2nnc(-c3c(-c4ccccc4)noc3C)o2)c1
Reaction #2070265
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1nnc(-c2c(-c3ccccc3)noc2C)o1
Reaction #2070266
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2nnc(-c3c(-c4ccccc4)noc3C)o2)cc1
Reaction #2070267
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1-c1nnc(-c2cccc3cccnc23)o1
Reaction #2070268
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1-c1nnc(-c2c(-c3ccccc3)noc2C)o1
Reaction #2070269
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1-c1nnc(-c2ccccn2)o1
Reaction #2070270
title compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2nnc(-c3c(-c4ccccc4)noc3C)o2)c(OC)c1
Reaction #2070271
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([N+](=O)[O-])ccc1-c1nnc(-c2c(-c3ccccc3)noc2C)o1
Reaction #2070272
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1-c1nnc(-c2ccccc2[N+](=O)[O-])o1
Reaction #2070273
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
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