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CCN(CC)C(N)=S

CC(=O)N1CCN(C(=S)Nc2cc3sc(C(C)(C)C)nc3cc2N2CCC(C)CC2)CC1
Reaction #5890
6-[(4-acetyl-piperazin-1-yl)thiocarbonylamino]-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
S=C1N(CCCc2ccncc2)CCN1CCc1ccccc1
Reaction #11565
titled compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(c2ccccc2)CCN(C(=S)Nc2ccc(Cl)cc2)CC1
Reaction #48555
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)O.S=C1NCCCN1CCCNCC1CCc2ccccc2O1
Reaction #51611
(±)-1-[3-[[(3,4-dihydro-2H-1-benzopyran-2-yl)methyl]amino]propyl]tetrahydro-2(1H)-pyrimidinethione ethanedioate
Ausbeute 7.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)N1CCN(c2cccc(CS(=O)(=O)C=C3CN(C(c4ccc(Cl)cc4)c4ccc(Cl)cc4)C3)c2)CC1
Reaction #53505
4-[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)phenyl]piperazine-1-carbothioic acid N-methylamide
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=S)n3ccnc3)C[C@H]2OC)nc1Cl
Reaction #71796
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(CC(=O)OC)c(C)s3)C[C@H]2OC)nc1Cl
Reaction #71797
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(c2csc(N3CC[C@H](NC(=O)c4nc(Cl)c(CC)[nH]4)[C@H](OC)C3)n2)CC1
Reaction #71799
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)sc1CC
Reaction #71803
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)sc1CC
Reaction #71810
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=S)N1CCOCC1
Reaction #80979
desired compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(N2CCOCC2)n1
Reaction #80980
desired compound
Ausbeute 55.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(N(CC)CC)n1
Reaction #80992
desired compound
Ausbeute 140.4%DOI: 10.6084/m9.figshare.5104873.v1
NC(=S)N1CCOCC1
Reaction #82214
desired compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(N2CCOCC2)n1
Reaction #82215
desired compound
Ausbeute 55.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=S)Nc2ccccc2Cc2ncc[nH]2)CC1
Reaction #179986
DOI: 10.1039/C8SC04228D
CCC(C)N(Cc1ccc(Cl)cc1)C(=S)Nc1ccccc1
Reaction #182449
DOI: 10.1039/C8SC04228D
CCC(=O)N1C(=S)N(c2cccc(C(F)(F)F)c2)C(C)=C(C(C)=O)C1c1ccc(C#N)cc1
Reaction #190287
DOI: 10.1039/C8SC04228D
COc1cc(OC)cc(N2CCN(C(=S)Nc3nc4ccccc4nc3OC)CC2)c1
Reaction #194973
DOI: 10.1039/C8SC04228D
Cc1ccc(C)c(NC(=S)N2CCC(c3nc(C4=NOC(c5ccccc5)C4)cs3)CC2)c1
Reaction #213107
DOI: 10.1039/C8SC04228D
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