guanidine

Cc1cc(C2C=CCC2)c(S(C)(=O)=O)cc1C(=O)N=C(N)N

N-diaminomethylene-2-methyl-4-(1-cyclopentene-3-yl)-5-methylsulfonylbenzamide

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03

CS(=O)(=O)c1cc(C(=O)N=C(N)N)ccc1C1C=CCC1

N-diaminomethylene-3-methylsulfonyl-4-(1-cyclopenten-3-yl)benzamide

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03

C=Cc1cc(C)c(C(=O)N=C(N)N)cc1S(C)(=O)=O

N-diaminomethylene-2-methyl-4-ethenyl-5-methylsulfonyl-benzamide

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03

N#Cc1cnc2nc(N)nc(N)c2c1

2,4-Diaminopyrido[2,3-d]pyrimidine-6-carbonitrile

수율 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02

CCCN(CCC)C1CCc2cccc(-c3ccnc(N)n3)c2C1

Reaction #50426

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06

N#Cc1ccc(Nc2nc(Cc3c(Cl)cccc3Cl)nc(NC(=N)N)n2)cc1

Reaction #53331

N-[4-[(4-cyanophenyl)amino]-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]-guanidine

수율 64.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02

COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OCC=C2

Reaction #62745

수율 42.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08

CCc1c(OC(C#N)=CNc2ccccc2)cc(C)c2sccc12

Reaction #66707

2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile

수율 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09

$C/C(=C\c1cc(F)c(Oc2ccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])cc2)c(F)c1)C(=O)N=C(N)N$

Reaction #73972

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09

Cc1nc(C)c(-c2ccnc(N)n2)s1

Reaction #75484

4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-ylamine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03

CCc1c(OC(C#N)=CNc2ccccc2)cc(C)c2sccc12

Reaction #169026

2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile

수율 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09

COc1cc(Cl)c([N+](=O)[O-])cc1N

Reaction #177739

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction #179190

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

COC(=O)CC(c1ccccc1)c1ccc(OC)c(S(=O)(=O)N=C(N)N)c1

Reaction #180713

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

O=C1CC(c2ccc(Cl)c([N+](=O)[O-])c2)CN1

Reaction #189814

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

N=C(N)NC(=O)c1cn(-c2nccc3ccccc23)c2ncccc12

Reaction #189829

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Cc1ccc(-c2cc(C)c(C(=O)N=C(N)N)cc2S(C)(=O)=O)cc1

Reaction #192988

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Cc1cc(N2CCCCC2)c(S(C)(=O)=O)cc1C(=O)N=C(N)N

Reaction #193109

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Cc1cc(S(F)(F)(F)(F)F)c(S(C)(=O)=O)cc1C(=O)NC(=N)N

Reaction #205762

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Cn1ccc2c(O)cc(Cc3cnc(N)nc3N)cc21

Reaction #212365

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

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