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CNC(N)=O

CC(=O)c1c(NC(=O)N(C)C)c2cc(-c3ccc(Cl)cc3)c(-c3ccc(Cl)cc3Cl)nc2n(C)c1=O
Reaction #42087
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]ccc23)c(-c2ccc(N(C)C(=O)Nc3ccccc3)cc2)n1
Reaction #57135
title product
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]c(-c4cccc(CN(C)C)c4)cc23)c(-c2ccc(NC(=O)N(C)C)cc2)n1
Reaction #57163
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1ccc(-c2nn(CC)cc2-c2ccnc3[nH]c(-c4cccc(CN(C)C)c4)cc23)cc1
Reaction #57173
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Nc1ccc(-c2nn(C)cc2-c2ccnc3[nH]c(-c4ccc(CN5CCCC5)cc4)cc23)cc1
Reaction #57175
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Nc1ccc(-c2n[nH]cc2-c2ccnc3[nH]c(-c4ccc(CN5CCCC5)cc4)cc23)cc1
Reaction #57177
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)Nc1ccc(-c2nn(CC)cc2-c2ccnc3[nH]c(-c4ccc(CN5CCCC5)cc4)cc23)cc1
Reaction #57179
title product
Ausbeute 37.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(C)CCn1cc(-c2ccnc3[nH]c(-c4cccc(CN(C)C)c4)cc23)c(-c2ccc(NC(=O)N(C)C)cc2)n1
Reaction #57183
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]c(-c4cccc(CN(C)C)c4)cc23)c(-c2ccc(NC(=O)N(C)C)cc2)n1
Reaction #57191
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOCCC1(Oc2ccc(Oc3ccc(CN)cc3)cc2)C(=O)NC(=O)NC1=O
Reaction #77433
5-[4-(4-aminomethyl-phenoxy)-phenoxy]-5-(2-ethoxy-ethyl)-pyrimidine-2,4,6-trione
Ausbeute 18.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nn(-c3c(Cl)cccc3Cl)c(=O)[nH]2)ccc1[N+](=O)[O-]
Reaction #87589
desired product
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=NOC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2)ccc1C(=O)NN1CCN(CC(F)(F)F)C1=O
Reaction #92112
4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydro-1,2-oxazol-3-yl]-2-methyl-N-[2-oxo-3-(2,2,2-trifluoroethyl)imidazolidin-1-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NC(=O)c1onc(-c2ccc(NC(=O)Nc3ccc(F)cc3)cc2)c1-c1ccccc1)C(C)C
Reaction #162974
title compound
Ausbeute 88.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc2ccc(N3CCN(c4cccnc4)C3=O)cc12
Reaction #167216
product
Ausbeute 35.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc3ccccc3c2)C1=O
Reaction #167221
1-(4-methyl-pyridin-3-yl)-3-naphthalen-2-yl-imidazolidin-2-one
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc3nc(Cl)cc(C)c3c2)C1=O
Reaction #167226
product
Ausbeute 46.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc3[nH]c(=O)cc(C)c3c2)C1=O
Reaction #167227
product
Ausbeute 80.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc3ncccc3c2)C1=O
Reaction #167259
product
Ausbeute 43.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(c2cncc(C(F)(F)F)c2)CCN1c1ccc2ccccc2c1
Reaction #167287
1-naphthalen-2-yl-3-(5-trifluoromethyl-pyridin-3-yl)-imidazolidin-2-one
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(c2c[nH]c3ccc(NC(=O)N(C)c4ccccc4)cc23)CC1
Reaction #176466
DOI: 10.1039/C8SC04228D
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