Substructure Search

38612

Nc1ccccc1NC(=O)c1cc(Cl)n[nH]c1=O
Reaction #40560
6-Chloro-3-oxo-2,3-dihydropyridazine-4-carboxylic acid (2-amino-phenyl)amide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Sc2[nH]c3ccccc3c2Cl)nn1
Reaction #51026
3-methoxy-6-(3-chloro-indole-2-sulfenyl)-pyridazine
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(C)nc1-c1ccc(NN)cc1
Reaction #75547
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1cc(=O)c(C(=O)OC)nn1-c1ccc(Cl)cc1
Reaction #95540
mixed products
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]nc2c3c(cccc13)NC(c1ncc[nH]1)C2c1ccc(F)cc1
Reaction #179579
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cc(NC(C)=O)ccc2nn1
Reaction #190509
DOI: 10.1039/C8SC04228D
FC(F)(F)c1cccc(CNc2ccc3c(Cl)nnc(Cl)c3c2)c1
Reaction #192465
DOI: 10.1039/C8SC04228D
Cc1cc2nc(C(C)(C)C(=O)OC(C)C)cn2nc1OCCCN1CCC(OC(c2ccccc2)c2ccccc2)CC1
Reaction #195067
DOI: 10.1039/C8SC04228D
Nc1ccccc1NC(=O)c1cc(Cl)n[nH]c1=O
Reaction #195750
DOI: 10.1039/C8SC04228D
Cc1cccc(-c2c(Cl)nnc(C)c2-c2ccc(Cl)cc2)n1
Reaction #205036
DOI: 10.1039/C8SC04228D
CCN(CC)Cc1ccc(C2Nc3cccc4c(=O)[nH]nc(c34)C2c2ccc(F)cc2)cc1
Reaction #206626
DOI: 10.1039/C8SC04228D
CN(C)Cc1cccc(C2Nc3cccc4c(=O)[nH]nc(c34)C2c2ccccc2)c1
Reaction #209157
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(-n2ncc3cccc(NCc4c[nH]c5ncccc45)c3c2=O)cc1
Reaction #220289
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nnc2c(c1Cl)CCCCC2
Reaction #226179
DOI: 10.1039/C8SC04228D
O=c1[nH]ncc(-c2ccc(Cl)cc2)c1-c1ccncc1
Reaction #229193
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(-n2ncc3cccc(NCc4c[nH]c5ncccc45)c3c2=O)cc1
Reaction #229684
DOI: 10.1039/C8SC04228D
O=Cc1ccc(C2Nc3cccc4c(=O)[nH]nc(c34)C2c2ccccc2)cc1
Reaction #229711
DOI: 10.1039/C8SC04228D
CCN1CCN(Cc2ccc(C3Nc4cccc5c(=O)[nH]nc(c45)C3c3ccccc3)cc2)CC1
Reaction #231775
DOI: 10.1039/C8SC04228D
O=c1ccc(-c2cc(F)cc(F)c2)nn1Cc1cccc(-c2noc(Cl)n2)c1
Reaction #232475
DOI: 10.1039/C8SC04228D
CCc1ccc2c(-c3cncc(C)c3)c(C(=O)O)c(C)nn12
Reaction #234259
DOI: 10.1039/C8SC04228D
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