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1171974

CN(C(=O)OC(C)(C)C)c1nc(N)c(C#CC2CCCCC2)c2c1ncn2C
Reaction #45393
tert-butyl 6-amino-7-(cyclohexylethynyl)-1-methyl-1H-imidazo[4,5-c]pyridin-4-yl(methyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(I)c2scc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45397
desired product
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)csc12
Reaction #45398
desired product
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)/C=C/c1cnc(N)c2c(C#CCOc3ccccc3)csc12
Reaction #45402
desired product
Выход 27.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(NC(=O)Nc2ccc(-c3csc4c(C#CCCO)cnc(N)c34)cc2)c1
Reaction #45413
desired product
Выход 82.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC/C=C/c1cnc(N)c2c(Br)csc12
Reaction #45415
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(I)c2scc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45418
desired product
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)csc12
Reaction #45419
desired product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)/C=C/c1cnc(N)c2c(Br)csc12
Reaction #45422
desired product
Выход 42.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(-c4cccc(N(C)C)c4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45454
title compound
Выход 20.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(I)cnc(N)c23)ccc1N
Reaction #45470
title compound
Выход 80.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(I)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45471
title compound
Выход 89.7%DOI: 10.6084/m9.figshare.5104873.v1
N#C/C=C/c1cnc(N)c2c(Br)csc12
Reaction #45475
title compound
Выход 88.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(-c4occc4C=O)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45476
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(-c4ccc(C=O)cc4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45477
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(-c4ccc(C=O)o4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45478
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(-c4ccsc4C=O)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45483
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(N=C(c4ccccc4)c4ccccc4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45510
title compound
Выход 64.8%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(I)c2onc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45523
title compound
Выход 64.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)noc12
Reaction #45524
7-[(1E)-3-(diethylamino)prop-1-enyl]-3-(4-phenoxyphenyl)isoxazolo[4,5-c]pyridin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
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