بحث البنية الفرعية

1184219

CC1CNc2cc(-c3cc(-c4ccc(S(=O)(=O)NC5CC5)cc4)cnc3N)ccc2C(=O)N1
Reaction #184853
DOI: 10.1039/C8SC04228D
Nc1ncc(-c2ccccc2)cc1-c1ccccc1
Reaction #338959
3,5-diphenyl-2-amino-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(-c2cn3cc(-c4ccccc4)ccc3n2)cc1
Reaction #338960
2-(4-bromo-phenyl)-6-phenyl-imidazo [1,2-a] pyridine
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)c1ccc(-c2cnc(N)c(-c3ccc4c(c3)CCNC4=O)c2)cc1
Reaction #377444
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(-c2cnc(N)c(-c3ccc(C(N)=O)cc3)c2)cc1
Reaction #658197
desired product
المردود 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(C)(C)c1ccc(-c2cnc(N)c(-c3ccc4c(c3)CCNC4=O)c2)cc1
Reaction #1219406
DOI: 10.1039/C8SC04228D
CC1(C)CNC(=O)c2ccc(-c3cc(-c4ccc(S(=O)(=O)NC5CC5)cc4)cnc3N)cc21
Reaction #1223497
DOI: 10.1039/C8SC04228D
COc1ccc(-c2cnc(N)c(-c3ccc(NC(=O)c4cn(C)cc(-c5ccc(F)cc5)c4=O)cc3)c2)cc1OC
Reaction #1515261
title compound
المردود 20.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc(N)c(-c3ccc(NC(=O)c4cn(CCOC5CCCCO5)cc(-c5ccc(F)cc5)c4=O)cc3)c2)cc1OC
Reaction #1515265
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(C(=O)Nc2ccc(-c3cc(-c4ccc(OC)c(OC)c4)cnc3N)cc2)c(=O)c(-c2ccccc2)c1
Reaction #1515274
title compound
المردود 74.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2cnc(N)c(-c3ccc(NC(=O)c4cn(CC(F)(F)F)cc(-c5ccc(F)cc5)c4=O)cc3)c2)c1
Reaction #1515282
title compound
المردود 10.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1cnc(N)c(-c2ccc(NC(=O)c3cn(CC(F)(F)F)cc(-c4ccc(F)cc4)c3=O)cc2)c1
Reaction #1515283
title compound
المردود 34.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cnc(N)c(-c3ccc(NC(=O)c4cn(CC(F)(F)F)cc(-c5ccc(F)cc5)c4=O)cc3)c2)ccc1O
Reaction #1515284
title compound
المردود 42.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cnc(N)c(-c3ccc(N)cc3)c2)ccc1OCCN1CCCC1
Reaction #1515286
title compound
المردود 105.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cnc(N)c(-c3ccc(N)cc3)c2)ccc1OC[C@H]1COCCO1
Reaction #1515288
title compound
المردود 60.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cnc(N)c(-c3ccc(NC(=O)c4cn(CCF)cc(-c5ccccc5)c4=O)cc3)c2)ccc1OC[C@H]1COCCO1
Reaction #1515290
title compound
المردود 77.8%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(C(=O)Nc2ccc(-c3cc(-c4ccc(OC[C@H]5COCCO5)c(OC)c4)cnc3N)cc2)c(=O)c(-c2ccccc2)c1
Reaction #1515291
title compound
المردود 53.8%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(C(=O)Nc2ccc(-c3cc(Br)cnc3N)cc2)c(=O)c(-c2ccc(F)cc2)c1
Reaction #1515292
title compound
المردود 242.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc(N)c(-c3ccc(NC(=O)c4cn(CC(F)(F)F)cc(-c5ccc(F)cc5)c4=O)cc3)c2)cc1OC.Cl
Reaction #1515310
title compound
المردود 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc(N)c(-c3ccc(NC(=O)c4cn(CC(F)(F)F)cc(-c5ccc(F)cc5)c4=O)cc3)c2)cc1OC.Cl
Reaction #1515311
title compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي