Substructure Search

822019

CC1(C)CNc2cc(Nc3ncnc4c3CN(c3ncccc3Cl)CC4)ccc21.Cl
Reaction #47925
HCl
Yield 236.3%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(C)(C)c2ccc(Nc3ncnc4c3CN(c3ncccc3Cl)CC4)cc21
Reaction #47926
solid
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(C2(c3ccc(N(C)C)cc3N(C)C)OC(=O)c3c(Cl)c(Cl)c(Cl)c(Cl)c32)c(C)c1
Reaction #55295
3-(2,4-bis(dimethylamino)phenyl)-3-(2-methyl-4-(diethylamino)phenyl)-4,5,6,7-tetrachlorophthalide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(C2(c3ccc(N(C)C)cc3N(C)C)OC(=O)c3c(Cl)c(Cl)c(Cl)c(Cl)c32)c(N(C)C)c1
Reaction #55296
3,3-bis(2,4-bis(dimethylamino)phenyl)-4,5,6,7-tetrachlorophthalide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(C2(c3ccc(N(C)C)cc3N(C)C)OC(=O)c3c(Cl)c(Cl)c(Cl)c(Cl)c32)cc1
Reaction #55303
3-(2,4-bis(dimethylamino)phenyl)-3-(4-(dimethylamino)phenyl)-4,5,6,7-tetrachlorophthalide
Yield 73.6%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(C2(c3ccc(N(C)C)cc3N(C)C)OC(=O)c3c(Cl)c(Cl)c(Cl)c(Cl)c32)cc1
Reaction #55305
3-(2,4-bis(dimethylamino)phenyl)-3-(4-(diethylamino)phenyl)-4,5,6,7-tetrachlorophthalide
Yield 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(C2(c3ccc(N(C)C)cc3)OC(=O)c3c(Cl)c(Cl)c(Cl)c(Cl)c32)c(N(CC)CC)c1
Reaction #55306
3-(2,4-bis(diethylamino)phenyl)-3-(4-(dimethylamino)phenyl)-4,5,6,7-tetrachlorophthalide
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(C2(c3ccc(N(CC)CC)cc3N(CC)CC)OC(=O)c3c(Cl)c(Cl)c(Cl)c(Cl)c32)cc1
Reaction #55307
3-(2,4-bis(diethylamino)phenyl)-3-(4-(diethylamino)phenyl)-4,5,6,7-tetrachlorophthalide
Yield 61.6%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(C2(c3ccc(N(CC)CC)cc3N(CC)CC)OC(=O)c3c(Cl)c(Cl)c(Cl)c(Cl)c32)c(C)c1
Reaction #55308
3-(2,4-bis(diethylamino)phenyl)-3-(2-methyl-4-(diethylamino)phenyl)-4,5,6,7-tetrachlorophthalide
Yield 52.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C(=O)[C@H]3CCCCN3)CC2)ccc1C#N)c1ccc(Cl)cc1Cl
Reaction #162319
desired product
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C(=O)[C@H]3CCCCN3)CC2)ccc1C#N)c1ccc(Cl)cc1Cl
Reaction #162320
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccc(N)cc1Nc1nc(Cl)ncc1Cl
Reaction #175017
DOI: 10.1039/C8SC04228D
CCN(CC)c1ccc(C2(c3ccc(N(C)C)cc3N(C)C)OC(=O)c3c(Cl)c(Cl)c(Cl)c(Cl)c32)c(C)c1
Reaction #179881
DOI: 10.1039/C8SC04228D
COc1ccc(CN2Cc3c(-c4ccccc4Cl)cc(NC4CCN(C(=O)OC(C)(C)C)CC4)cc3N(c3c(Cl)cccc3Cl)C2=O)cc1
Reaction #184977
DOI: 10.1039/C8SC04228D
Cc1ccc(-n2nc(C(C)(C)C)cc2NC(=O)Nc2ccc(C)c(NC(=O)c3ccc(=O)n(-c4c(Cl)cccc4Cl)c3)c2)cc1
Reaction #192453
DOI: 10.1039/C8SC04228D
COc1ccc(CN2Cc3c(-c4ccccc4Cl)cc([N+](=O)[O-])cc3N(c3c(Cl)cccc3Cl)C2=O)cc1
Reaction #232164
DOI: 10.1039/C8SC04228D
O=C(Nc1cc([N+](=O)[O-])ccc1C(=O)O)OCC(Cl)(Cl)Cl
Reaction #233325
DOI: 10.1039/C8SC04228D
CC(C)(C)N1CCC(Nc2cc(-c3ccccc3Cl)c3c(c2)N(c2c(Cl)cccc2Cl)C(=O)NC3)CC1
Reaction #234807
DOI: 10.1039/C8SC04228D
COc1ccc(CN2Cc3c(-c4ccccc4Cl)cc(N)cc3N(c3c(Cl)cccc3Cl)C2=O)cc1
Reaction #258817
DOI: 10.1039/C8SC04228D
CNC(=O)c1ccc([N+](=O)[O-])cc1Nc1nc(Nc2ccc3c(c2)C(C)(C)CCC(=O)N3)ncc1Cl
Reaction #271971
DOI: 10.1039/C8SC04228D
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