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c1ccc(Cn2cccn2)cc1

CSc1nc(=O)c2cnn3c2n1CC=C3c1cccc(C(F)(F)F)c1
Reaction #6314
desired product
Выход 90.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Nc1nc(=O)c2cnn3c2n1CC=C3c1cccc(C(F)(F)F)c1
Reaction #6315
desired product
Выход 62.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc2c(/C=C/c3ccc4c(c3)OCO4)nn(C(c3ccccc3)(c3ccccc3)c3ccccc3)c2cc1F
Reaction #62378
title compound
Выход 13.8%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1cnn(Cc2ccc(OC)cc2)c1
Reaction #66509
1-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)propan-1-one
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2cc(C(=O)CC#N)cn2)cc1
Reaction #66511
3-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-3-oxopropanenitrile
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(cnn2Cc2cccc(F)c2)c1
Reaction #66789
title compound
Выход 64.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1Cc2sc3ncnc(Nc4ccc5c(cnn5Cc5cccc(F)c5)c4)c3c2C1
Reaction #66808
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc(Cn2ncc3cc(Nc4ncnc5sc6c(c45)CCCNC6)ccc32)c1
Reaction #66842
title compound
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2c(sc3ncc(C#N)c(Nc4ccc5c(cnn5Cc5cccc(F)c5)c4)c23)C1
Reaction #66848
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(C(c2ccccc2)(c2ccccc2)n2ncc3c(-c4cn[nH]c4)ccnc32)cc1
Reaction #72957
compound
Выход 49.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCn1cc(-c2ccnc3c2cnn3C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1
Reaction #72958
2-(4-(1-trityl-1H-pyrazolo[3,4-b]pyridin-4-yl)-1H-pyrazol-1-yl)ethanenitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C#N)n1cc(-c2ccnc3[nH]ncc23)cn1
Reaction #72959
product
Выход 57.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(c2ccc(OC)cc2)(c2ccc(OC)cc2)n2cc(-c3ccc(C(OC)C(=O)N(C)OC)cc3)cn2)cc1
Reaction #84790
N,2-dimethoxy-N-methyl-2-(4-(1-(tris(4-methoxyphenyl)methyl)-1H-pyrazol-4-yl)phenyl)acetamide
Выход 37.5%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)c2c(Oc3ccccc3)n(Cc3ccc(-c4ccncc4)cc3)nc2n(CC(C)(C)C)c1=O
Reaction #85938
pure product
Выход 67.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2n(-c3ccccc3)c(=O)c3cnc4c(cnn4C(=O)c4ccccc4)c3n2n1
Reaction #93982
8-Benzoyl-2-methyl-4-phenyl-4H-pyrazolo[1,5-a]pyrazolo[4',3':5,6]pyrido[3,4-e]pyrimidin-5(8H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2nc(CO)c3ccccc32)cc1
Reaction #163293
[1-(4-methoxybenzyl)-1H-indazol-3-yl]methanol
Выход 27.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc2c1c(I)nn2Cc1ccccc1
Reaction #166438
1-benzyl-3-iodo-1H-indazol-4-amine
Выход 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccn2c(C(=O)Nc3cccc4c3c(I)nn4Cc3ccccc3)cnc2c1
Reaction #166439
N-(1-Benzyl-3-iodo-1H-indazol-4-yl)-7-(2-methoxyethoxy)imidazo[1,2-a]pyridine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2ccccc2)c2cccc(NC(=O)c3cnc4cc(OCCOC)ccn34)c12
Reaction #166442
N-(1-benzyl-3-ethyl-1H-indazol-4-yl)-7-(2-methoxyethoxy)imidazo[1,2-a]pyridine-3-carboxamide
Выход 18.8%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccn2c(C(=O)Nc3cccc4c3c(C3CC3)nn4Cc3ccccc3)cnc2c1
Reaction #166447
N-(1-benzyl-3-cyclopropyl-1H-indazol-4-yl)-7-(2-methoxyethoxy)imidazo[1,2-a]pyridine-3-carboxamide
Выход 29.1%DOI: 10.6084/m9.figshare.5104873.v1
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