Substructure Search

349186

NC1=Nc2ccc(-c3cccc(Cl)c3)cc2C12CCCCC2
Reaction #9434
desired product
Yield 130.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(c1cnc(C(C)(C)C)nc1)C(C)C
Reaction #62876
ethyl (RS)-2-[2-(2-methylprop-2-yl)pyrimidin-5-yl]-3-methylbutyrate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(COCCCl)C(=N)NO
Reaction #230765
DOI: 10.1039/C8SC04228D
CN(C)C(=Nc1ccc(Cl)nn1)C(C)(C)C
Reaction #276641
DOI: 10.1039/C8SC04228D
CC(C)(C)c1nc(-c2ccc(Br)cc2)c[nH]1
Reaction #310111
title compound
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=Nc2ccc(-c3cccc(Cl)c3)cc2C12CCCCC2
Reaction #364187
desired product
Yield 130.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(N)sc1-c1ccnc(C2(C)CC2)n1
Reaction #532068
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(N)sc1-c1ccnc(C(C)(C)C(F)(F)F)n1
Reaction #532071
4-Methyl-5-[2-(2,2,2-trifluoro-1,1-dimethyl-ethyl)-pyrimidin-4-yl]-thiazol-2-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
NC1=Nc2ccc(-c3cccc(Cl)c3)cc2C12CCCCC2
Reaction #583874
desired product
Yield 130.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(C(C)(C)C)nc1O
Reaction #686497
ethyl 2-tert-butyl-4-hydroxypyrimidine-5-carboxylate
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=NC(=O)c2ccc(Cl)cc2)C(C)(C)c2ccccc21
Reaction #750275
DOI: 10.1039/C8SC04228D
Cc1c(Cl)c(C(F)(F)F)nn1CC(=O)N1CCC(C(N)=O)(c2ccc(Cl)cc2)CC1
Reaction #752197
DOI: 10.1039/C8SC04228D
CC(C)(COCCCl)C(=N)NO
Reaction #766505
DOI: 10.1039/C8SC04228D
CC(C)(c1cccc(C(F)(F)F)c1)c1nnc(Cn2nc(-c3ccc(Cl)cc3)n(C3CC3)c2=O)[nH]1
Reaction #801865
5-(4-Chlorophenyl)-4-cyclopropyl-2-[(5-{2-[3-(trifluoromethyl)phenyl]propan-2-yl}-4H-1,2,4-triazol-3-yl)methyl]-2,4-dihydro-3H-1,2,4-triazol-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1nnc(Cn2nc(-c3ccc(Cl)cc3)n(C3CC3)c2=O)[nH]1)c1ccccc1F
Reaction #801866
5-(4-Chlorophenyl)-4-cyclopropyl-2-({5-[1-(2-fluorophenyl)-1-methylethyl]-4H-1,2,4-triazol-3-yl}methyl)-2,4-dihydro-3H-1,2,4-triazol-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1nc(-c2ccc(Br)cc2)c[nH]1
Reaction #817564
title compound
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=N)Nc1ccc(Br)cc1F)c1c(Cl)cccc1Cl
Reaction #1036229
DOI: 10.1039/C8SC04228D
CC1C=CC2=C(C1=O)C(C(=O)[C@H](C)NC(=O)[C@@H](O)c1cc(F)cc(F)c1)CC(C)(C)C(N)=N2
Reaction #1052932
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCCNC1=N.Cl
Reaction #1090627
3,3-dimethylpiperidin-2-imine, monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
NC1=Nc2ccc(-c3cccc(Cl)c3)cc2C12CCCCC2
Reaction #1147238
desired product
Yield 130.4%DOI: 10.6084/m9.figshare.5104873.v1
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