部分構造検索

797857

CC(C)(C)OC(=O)N1CCN(c2cc(-c3cc(Cl)ccc3O)ccn2)CC1
Reaction #74652
product
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(C)[nH]c(=O)c1CNC(=O)c1cc(-c2ccnc(N3CCN(C)CC3)c2)cc2c1c(C)nn2C(C)C
Reaction #172667
title compound
収率 32.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(CNC(=O)c2cc(-c3cccc(N4CCN(C)CC4)n3)cc3c2c(C)nn3C(C)C)c(=O)[nH]1
Reaction #172675
title compound
収率 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2cc(-c3cnc4c(c3)N(Cc3ccc(C(F)(F)F)o3)CCN4)ccn2)CC1
Reaction #240648
DOI: 10.1039/C8SC04228D
CN1CCN(c2cc(-c3cnc4c(c3)C(Oc3cccc(Cl)c3)CCN4)ccn2)CC1
Reaction #250384
DOI: 10.1039/C8SC04228D
CN1CCN(c2cc(-c3ccc4c(c3)CN(c3cc(N5CCN(C)CC5)nc(N)n3)CC4)ccn2)CC1
Reaction #270631
DOI: 10.1039/C8SC04228D
Clc1cnc2nc1Nc1cccc(c1)OCCc1cc(cc(-c3ccnc(N4CCNCC4)c3)c1)N2.O=C(O)C(F)(F)F.O=C(O)C(F)(F)F.O=C(O)C(F)(F)F
Reaction #629119
desired product
収率 40.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2cc(-c3cnc4c(c3)N(Cc3c(F)ccc(F)c3Cl)CCN4)ccn2)CC1
Reaction #746619
title compound
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2cc(-c3cnc4c(c3)C(Oc3cccc(Cl)c3)CCN4)ccn2)CC1
Reaction #746643
title compound
収率 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2cc(-c3cnc4c(c3)N(Cc3ccc(C(F)(F)F)o3)CCN4)ccn2)CC1
Reaction #746657
title compound
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cc(-c3cc(Cl)ccc3O)ccn2)CC1
Reaction #751330
DOI: 10.1039/C8SC04228D
CN1CCN(c2cc(-c3ccc(S(=O)(=O)n4ccc(C=CC(=O)NOC5CCCCO5)c4)cc3)ccn2)CC1
Reaction #918843
DOI: 10.1039/C8SC04228D
COc1cc(CCc2cnc3[nH]c(-c4ccnc(N5CCN(C)CC5)c4)cc3n2)cc(OC)c1
Reaction #1139457
2-(3,5-Dimethoxyphenethyl)-6-(2-(4-methylpiperazin-1-yl)pyridin-4-yl)-5H-pyrrolo[2,3-b]pyrazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cc(-c3cc(Cl)ccc3O)ccn2)CC1
Reaction #1489226
product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccnc(N3CCN(C)CC3)c2)nc2cc(F)cc(F)c2c1Cl
Reaction #1518920
4-chloro-5,7-difluoro-3-methyl-2-(2-(4-methylpiperazin-1-yl)pyridin-4-yl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2cc(-c3ccc(S(=O)(=O)n4ccc(/C=C/C(=O)NOC5CCCCO5)c4)cc3)ccn2)CC1
Reaction #1532678
title compound
収率 64.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(C)[nH]c(=O)c1CNC(=O)c1cc(-c2ccnc(N3CCN(C)CC3)c2)cc2c1c(C)nn2C(C)C
Reaction #1563632
title compound
収率 32.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(CNC(=O)c2cc(-c3cccc(N4CCN(C)CC4)n3)cc3c2c(C)nn3C(C)C)c(=O)[nH]1
Reaction #1563640
title compound
収率 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cc(-c3cc(Cl)ccc3O)ccn2)CC1
Reaction #1779521
product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(F)c(-c2ncc3c(-c4ccnc(N5CCN(C)CC5)c4)n[nH]c3n2)c1F
Reaction #1865859
6-(2,6-Difluoro-3,5-dimethoxyphenyl)-3-[2-(4-methylpiperazin-1-yl)pyridin-4-yl]-1H-pyrazolo[3,4-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
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