Substructure Search

C(=O)(N)N

Cc1ccc2c(N3CCN(CCc4cccc(N5CCN(C)C5=O)c4)CC3)cccc2n1
Reaction #44139
final compound
Yield 45.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cc(N5CCNC5=O)ccc4F)CC3)cccc2n1
Reaction #44149
title compound
Yield 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2cccc(CCN3CCN(c4cccc5nc(C)ccc45)CC3)c2)C1=O.Cl
Reaction #44164
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1OS(=O)(=O)NC(=O)Nc1nc(OC)cc(OC)n1
Reaction #64667
desired product
Yield 97.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(NC(=O)NC(=O)c2ccccc2)c1C#N
Reaction #72665
N-(2-cyano-3-methoxyphenylcarbamoyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN(C(=O)N[C@@H](C)c2ccc(Cl)cc2)c2ccc(C3CCCCC3)cc2)cc1
Reaction #77823
4-[3-[1(S)-(4-Chlorophenyl)ethyl]1-(4-cyclohexylphenyl)ureidomethyl]benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)N(Cc1ccc(C(=O)O)cc1)c1ccc(C2CCCCC2)cc1)c1ccc(Cl)cc1
Reaction #77824
4-[3-[1(S)-(4-Chlorophenyl)ethyl]1-(4-cyclohexylphenyl)ureidomethyl]benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)N(c2ccccc2)C(=O)N1c1ccccc1
Reaction #162817
1,3-diphenyl-pyrimidine-2,4,6-trione
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(Cl)n(-c2ccccc2)c(=O)n1-c1ccccc1
Reaction #162818
6-chloro-1,3-diphenyl-1H-pyrimidine-2,4-dione
Yield 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC1(c2ccc(I)cc2)CCN(CC2CC2)CC1)C(=O)Nc1cc(Cl)cc(Cl)c1
Reaction #174975
DOI: 10.1039/C8SC04228D
N#Cc1ccc(-c2ccc(N)cc2)nc1Cl
Reaction #177610
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(C(=O)O)cc1)Nc1ccc(-c2nc(N3CCOCC3)nc(N3CCOCC3)n2)cc1
Reaction #183002
DOI: 10.1039/C8SC04228D
CN1CC(c2ccc(NC(=O)c3cc(C#N)c[nH]3)c(C3=CCCCCC3)c2)CN(C)C1=O
Reaction #183958
DOI: 10.1039/C8SC04228D
Cc1c(Cc2ccccc2)c(=O)oc2cc(OC(=O)N3CCCc4ccccc43)ccc12
Reaction #184067
DOI: 10.1039/C8SC04228D
CC(NC(=O)C(O)C(CCCCNC(=O)N1CCOCC1)NC(=O)OCC1(Cc2ccccc2)CCCCC1)c1ccccc1
Reaction #185342
DOI: 10.1039/C8SC04228D
O=C(Oc1ccc(Oc2ncc(Cl)cc2Cl)cc1)N1CCCc2ccccc21
Reaction #190225
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(N2CCOCC2=O)cc1)C1CC(O)CN1C(=O)Nc1ccc(Cl)cc1
Reaction #197509
DOI: 10.1039/C8SC04228D
ClCCN1C(Cl)=Nc2ccc(Cl)cc2C1c1ccccc1
Reaction #204350
DOI: 10.1039/C8SC04228D
O=C1N(CCO)CCN1c1ccc(C(F)(F)F)cc1
Reaction #206822
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(NC(=O)CC(C(=O)Nc2ccc(NC(=O)Nc3ccccc3C)cc2)c2ccccc2)cc1
Reaction #207141
DOI: 10.1039/C8SC04228D
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