Substructure Search

CCc1ccc(Cl)cc1

CN1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #1680
product
DOI: 10.6084/m9.figshare.5104873.v1
CN1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #2185
product
DOI: 10.6084/m9.figshare.5104873.v1
CN1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #2226
product
DOI: 10.6084/m9.figshare.5104873.v1
CN1N=C(c2ccc(Cl)cc2)CCC1=O
Reaction #2284
product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1c(-c2ccc(OCCc3ccc(Cl)cc3)cc2)nc2ccc(OCCN3CCCC3)cc21
Reaction #45921
1-butyl-2-{4-[2-(4-chlorophenyl)ethoxy]-phenyl}-6-(2-pyrrolidin-1-yl-ethoxy)-1H-benzimidazole
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(CC1CNC1)c1ccccc1
Reaction #46339
3-(phenylsulfonylmethyl)azetidine
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(C(C[C@H]2CCC(=O)N2)c2ccc(Cl)cc2)ccc1-c1cn[nH]c1
Reaction #157875
(5R)-5-{2-(4-chlorophenyl)-2-[6-methoxy-5-(1H-pyrazol-4-yl)pyridin-2-yl]ethyl}pyrrolidin-2-one
Yield 62.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(c1ccc(Cl)cc1)=N[C@@H](CC(=O)O)c1nnc(C)n1-2
Reaction #169200
title compound
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCC(C(=O)N1CCN(c2ncnc3c2[C@H](C)CC3)CC1)c1ccc(Cl)cc1.Cl.Cl
Reaction #169534
2-(4-chlorophenyl)-3-(isopropylamino)-1-(4-((R)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)piperazin-1-yl)propan-1-one dihydrochloride
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC[C@@H](C(=O)N1CCN(c2ncnc3c2[C@H](C)CC3)CC1)c1ccc(Cl)cc1.Cl.Cl
Reaction #169551
(S)-2-(4-chlorophenyl)-3-(isopropylamino)-1-(4-((R)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)piperazin-1-yl)propan-1-one dihydrochloride
Yield 189.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCc2ncnc(N3CCN(C(=O)[C@H](CN)c4ccc(Cl)cc4)CC3)c21.Cl.Cl
Reaction #169572
(S)-3-amino-2-(4-chlorophenyl)-1-(4-((R)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)piperazin-1-yl)propan-1-one dihydrochloride
Yield 157.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nccs1)C1C(=O)Sc2cc(Cl)ccc21
Reaction #174563
DOI: 10.1039/C8SC04228D
CC(C)(C)CC1NC(C(=O)Nc2ccn(CC(C)(C)OCC(O)CO)n2)C(c2cccc(Cl)c2F)C1(C#N)c1ccc(Cl)cc1F
Reaction #177403
DOI: 10.1039/C8SC04228D
CC(C)(C)CC1NC(C(=O)Nc2ccn(CC(C)(C)O)n2)C(c2cccc(Cl)c2)C1(C#N)c1ccc(Cl)cc1
Reaction #179571
DOI: 10.1039/C8SC04228D
Cl
Reaction #179721
DOI: 10.1039/C8SC04228D
CN1CC2Cc3ccc(Cl)cc3C(=O)C2C1
Reaction #186170
DOI: 10.1039/C8SC04228D
CN1CC2Cc3ccc(Cl)cc3C(O)C2C1
Reaction #203706
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(Cc2ccc(Cl)c(Cl)c2)CC1
Reaction #210592
DOI: 10.1039/C8SC04228D
O=C1C(O)=C(C2CCC(c3ccc(Cl)cc3)CC2)C(=O)c2ccccc21
Reaction #216207
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CC1NC(C(=O)Nc2ccn(CCO)n2)C(c2cccc(Cl)c2)C1(C#N)c1ccc(Cl)cc1
Reaction #232944
DOI: 10.1039/C8SC04228D
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