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C(=O)(N)NN.Cl

CS(=O)(=O)Cc1ccc(C(=NNC(N)=O)c2ccc(Cl)cc2)cc1
Reaction #2190
desired product
Ausbeute 81.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1)Nc1ccc(Cl)cc1
Reaction #4711
N-4-Chlorophenyl-2-[[3-[3-(1-piperidinylmethyl)phenoxy]propyl]aminothioxomethyl]-hydrazine carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCOc1cccc(CN2CCCCC2)c1)NNC(=O)Nc1ccc(Cl)cc1
Reaction #4720
N-4-Chlorophenyl-N'-[3-[3-(1-piperidinylmethyl)-phenoxy]propyl]-1,2-hydrazine dicarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Nc2nnc(NCCCOc3cccc(CN4CCCCC4)c3)o2)cc1
Reaction #4731
N-4-Chlorophenyl-N'-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-1,3,4-oxadiazole-2,5-diamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@H](O)CS(=O)(=O)c1ccc2cc(Cl)ccc2c1)N1CCN(N2CCCNC2=O)CC1
Reaction #48508
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C(=O)N(NC(=O)NS(=O)(=O)c2ccc(Cl)cc2)C(C)(C)C)c1
Reaction #49952
1-t-butyl-1-(3-toluoyl)-4-(4-chlorobenzenesulfonyl)semicarbazide
DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C(=O)NCCCl)OCO3
Reaction #53339
title compound
Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C1=NCCO1)OCO3
Reaction #53349
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCCN1N=C1CC=C(Cl)O1
Reaction #54202
1-(5-Chlorofurylideneamino)- 2-oxo-imidazolidine
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCC(=N)N)C(=O)c1cc(N(C)C(=O)c2cc(NC(=O)N(C)N=O)c[nH]2)c[nH]1.Cl
Reaction #63552
β-[N-methyl-4-[N-methyl-4-(3 -methyl-3-nitrosoureido)pyrrole-2-carboxamido]pyrrole-2-carboxamido]propionamidine hydrochloride
Ausbeute 55.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(-c2cc(OC(C)C)c(Cl)cc2Cl)c(=O)[nH]c1=O
Reaction #63700
2-[2,4-dichloro-5-(1-methylethoxy)phenyl]-6-methyl-1,2,4-triazine-3,5(2H,4H)-dione
Ausbeute 58.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]nc(N)c1-c1ccc(Sc2ccccc2)cc1
Reaction #65409
title compound
Ausbeute 91.4%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1C[C@@H](c2n[nH]c(=O)[nH]2)C[C@@H]1O[N+](=O)[O-]
Reaction #69437
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1-c1ccc(N2CCCC(Nc3cccc(-c4n[nH]c(=O)[nH]4)c3)C2=O)c(F)c1
Reaction #78319
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc(CN(N)C(=O)N[C@H](C(=O)N[C@@H](Cc2ccccc2)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)OCc2cncs2)C(C)C)cs1.Cl
Reaction #81012
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc(CN(N)C(=O)N[C@H](C(=O)N[C@@H](Cc2ccccc2)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)OCc2cncs2)C(C)C)cs1.Cl
Reaction #84004
desired compound
Ausbeute 77.0%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
O=C1CN(Nc2nc(Cl)nc(Cl)n2)C(=O)N1
Reaction #163513
crude product
Ausbeute 107.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NNC(=O)Nc2cc(Cl)cc(Cl)c2)nc2c(C)cccc12
Reaction #174298
DOI: 10.1039/C8SC04228D
O=NN(CCCl)C(=O)NC1OC(CO)C(O)C(O)C1O
Reaction #175846
DOI: 10.1039/C8SC04228D
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