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169498

C[C@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1cccc(Br)c1
Reaction #43246
desired product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1cccc(-c2ccnc(Cl)n2)c1
Reaction #43247
(3S)-tert-butyl 4-(3-(2-chloropyrimidin-4-yl)phenylsulfonyl)-3-methylpiperazine-1-carboxylate
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CNCCN1S(=O)(=O)c1cccc(-c2ccnc(NCCc3cccc(F)c3)n2)c1
Reaction #43248
N-(3-fluorophenethyl)-4-(3-((S)-2-methylpiperazin-1-ylsulfonyl)phenyl)pyrimidin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CNCCN1S(=O)(=O)c1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43249
4-(2-(4-(3-((S)-2-methylpiperazin-1-ylsulfonyl)phenyl)pyrimidin-2-ylamino)ethyl)phenol
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #69571
title compound
Ausbeute 129.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CNCCN1S(=O)(=O)c1ccc(Cl)cc1.Cl
Reaction #69572
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #69574
title compound
Ausbeute 110.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CNCCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1.Cl
Reaction #69575
title compound
Ausbeute 87.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #69576
title compound
Ausbeute 105.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CNCCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1.Cl
Reaction #69577
title compound
Ausbeute 102.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #71643
title compound
Ausbeute 129.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CNCCN1S(=O)(=O)c1ccc(Cl)cc1.Cl
Reaction #71644
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #71645
title compound
Ausbeute 110.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CNCCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1.Cl
Reaction #71646
title compound
Ausbeute 87.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #71647
title compound
Ausbeute 105.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CNCCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1.Cl
Reaction #71648
title compound
Ausbeute 102.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)ccc1S(=O)(=O)N1CCNC[C@@H]1C
Reaction #71652
title compound
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=S(=O)(c1ccccc1)N1CCNCC1COc1cccnc1
Reaction #157407
desired product
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #190831
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)N2CC(CC(C)C)N(C(=O)OC(C)(C)C)CC2CO)cc1
Reaction #197764
DOI: 10.1039/C8SC04228D
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