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416993

CS(=O)c1cncc2cccc(NC3CCN(C(=O)OC(C)(C)C)CC3)c12
Reaction #10632
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)c1cncc2cccc(NC3CCNCC3)c12.Cl
Reaction #10633
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cncc2cccc(NC3CCNCC3)c12.Cl
Reaction #10634
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2nccc3c(NC4CCN(C(=O)OC(C)(C)C)CC4)cccc23)cc1
Reaction #10676
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Nc2cccc3c(N)nccc23)CC1
Reaction #10677
title compound
Ausbeute 99.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Nc2nc(N)c(C(=O)c3cccc(F)c3)s2)CC1
Reaction #58432
4-[4-amino-5-(3-fluorobenzoyl)thiazol-2-ylamino]piperidine-1-carboxylic acid tert-butyl ester
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NC2CCNCC2)sc1C(=O)c1cccc(F)c1
Reaction #58433
[4-amino-2-(piperidin-4-ylamino)thiazol-5-yl]-(3-fluorophenyl)methanone
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1nc(Cl)c(C(C)C)[nH]1
Reaction #71743
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2OCC(C)(F)F)nc1Cl
Reaction #71991
title compound
Ausbeute 94.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=O)OC(C)(C)C)C[C@H]2N(C)C)nc1Cl
Reaction #72122
title compound
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](N(C)C)C2)nc1C
Reaction #72123
title compound
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](NCc3ccccc3)C2)nc1C
Reaction #72132
title compound
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc2nc(N3CC[C@H](NC(=O)c4nc(Cl)c(CC)[nH]4)[C@H](NC(CC)CC)C3)sc12
Reaction #72148
title compound
Ausbeute 18.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc2nc(N3CC[C@@H](NC(=O)c4nc(Cl)c(CC)[nH]4)[C@H](NC(CC)CC)C3)sc12
Reaction #72149
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@H](NC(=O)OCc2ccccc2)[C@H](NC(=O)c2ccc(S(N)(=O)=O)cc2)C1
Reaction #77839
tert-butyl (cis)-3-{[4-(aminosulfonyl)benzoyl]amino}-4-{[(benzyloxy)carbonyl]amino}-1-piperidinecarboxylate
Ausbeute 45.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NS(=O)(=O)c1ccc(CN(CCc2ccc(Br)cc2)C2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #88069
tert-butyl 4-((4-(N-acetylsulfamoyl)benzyl)(4-bromophenethyl)amino)piperidine-1-carboxylate
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NS(=O)(=O)c1ccc(CN(CCc2ccc(Br)cc2)C2CCNCC2)cc1.Cl
Reaction #88070
N-((4-(((4-bromophenethyl)(piperidin-4-yl)amino)methyl)phenyl)sulfonyl)acetamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CC(C(F)(F)F)n3nc(-c4ccnc(C(=O)NC5CCN(C(=O)OC(C)(C)C)CC5)c4)cc3N2)cc1OC
Reaction #90493
tert-butyl 4-(4-(5-(3,4-dimethoxyphenyl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-2-yl)picolinamido)piperidine-1-carboxylate
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nn(-c2ccccc2)c2cc(N3CCN(C4CCNCC4)CC3)ccc12.Cl
Reaction #155892
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNC(=O)c2cc(OCc3ccccc3)ccc2N(C(=O)OCC(C)C)C2CCN(C(=O)OC(C)(C)C)CC2)cc1OC
Reaction #167645
expected product
DOI: 10.6084/m9.figshare.5104873.v1
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