Substructure Search

5306

c1cc(-c2ccc(-c3ccc(C4=NCCCCN4)cc3)o2)ccc1C1=NCCCCN1
Reaction #890
2,5-bis [4-(4,5,6,7-tetrahydro-1H-1,3-diazepin-2-yl) phenyl] furan
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(NCCc4ccccc4)c(=O)n32)cc1
Reaction #11053
intermediate 2a
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OC(C)(C)C)cc1)CC2
Reaction #11054
intermediate 3a
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Nc1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OC(C)(C)C)cc1)CC2
Reaction #11055
intermediate 4a
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OC(C)(C)C)cc1)CC2
Reaction #11056
intermediate 5a
Yield 60.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(NC4CCCC4)c(=O)n32)cc1
Reaction #11057
intermediate 6a
Yield 57.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNc1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OC(C)(C)C)cc1)CC2
Reaction #11058
intermediate 7a
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCNc1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OC(C)(C)C)cc1)CC2
Reaction #11059
intermediate 8a
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CN(CC(C)C)c1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OC(C)(C)C)cc1)CC2
Reaction #11060
intermediate 9a
Yield 79.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)Nc1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OC(C)(C)C)cc1)CC2
Reaction #11061
intermediate 11a
Yield 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(NS(C)(=O)=O)c(=O)n32)cc1
Reaction #11062
intermediate 16a
Yield 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(NS(=O)(=O)c4ccccc4)c(=O)n32)cc1
Reaction #11063
intermediate 17a
Yield 80.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)NCC
Reaction #11084
26b
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)NC(C)C
Reaction #11085
27a
Yield 28.1%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1cccc2ccccc12
Reaction #11090
1-napthalene sulfonamide
Yield 30.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)Nc2cnc3n(c2=O)[C@H](C(=O)NCc2ccc(C(=N)NC(=O)OC(C)(C)C)cc2)CC3)cc1
Reaction #11091
31a
Yield 46.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(NS(=O)(=O)c4ccc(F)cc4)c(=O)n32)cc1
Reaction #11092
32a
Yield 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(NS(=O)(=O)c4ccc(OC(F)(F)F)cc4)c(=O)n32)cc1
Reaction #11093
33a
Yield 41.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(S(=O)(=O)Nc2cnc3n(c2=O)[C@H](C(=O)NCc2ccc(C(=N)NC(=O)OC(C)(C)C)cc2)CC3)cc1
Reaction #11094
35a
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(NS(=O)(=O)Cc4ccccc4)c(=O)n32)cc1
Reaction #11095
36a
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1
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