1H-benzimidazol-2-amine

c1cnc2c(c1)CCCC2N(Cc1ccc(CNc2nc3ccccc3[nH]2)cc1)Cc1nc2ccccc2[nH]1
Reaction #7279
{4-[(1H-Benzimidazol-2-ylamino)-methyl]-benzyl}-(1H-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CS(=O)(=O)n1c(N)nc2ccccc21
Reaction #57425
N-methanesulfonyl-2-aminobenzimidazole
Ausbeute 28.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)ccc1C(=O)Nc1nc2ccccc2[nH]1
Reaction #87739
desired product
Ausbeute 32.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(=O)OCC1OC(NC(=S)Nc2nc3ccccc3[nH]2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #173508
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)c1ccc(C(CC2CCCC2)C(=O)Nc2nc3ccccc3[nH]2)cc1Br
Reaction #177702
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Br
Reaction #189824
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCC(=O)n1c(N)nc2ccccc21
Reaction #191494
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
S=C(Nc1nc2ccccc2[nH]1)n1ccnc1
Reaction #204060
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1nc2ccccc2n1Cc1cccc(F)c1
Reaction #223824
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1ccc([N+](=O)[O-])c(N)c1
Reaction #230136
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Nc1nc2ccccc2[nH]1)C(CC1CCCC1)c1ccc(Cl)c(Cl)c1
Reaction #236783
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cccnc1CN(Cc1ncccc1C)C1CCN(C(=O)Nc2nc3ccccc3[nH]2)CC1
Reaction #240549
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(C)S(=O)(=O)c1cccc2nc(N)[nH]c12
Reaction #244852
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1nc2ccccc2n1-c1ncnc(Cl)n1
Reaction #251349
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCN(CC)c1ccc(C(=O)Cn2c(N)nc3ccccc32)cc1
Reaction #256166
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCN1C(=O)C(Nc2nc3ccccc3[nH]2)=C(c2ccccc2)S1(=O)=O
Reaction #262783
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC=CC=CC(=O)n1c(N)nc2ccccc21
Reaction #283848
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1c2ccccc2C(=O)N1c1nc2ccccc2[nH]1
Reaction #290448
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cn1c(N)nc2ccccc21
Reaction #297918
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1nc2ccccc2n1N
Reaction #299397
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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