Teilstruktursuche

831153

Cc1cc(C(=O)N2CCN(S(=O)(=O)c3ccc(C(F)(F)F)cc3)CC2)ccn1
Reaction #69591
title compound
Ausbeute 57.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)N2CCN(S(=O)(=O)c3ccc(C(F)(F)F)cc3)C[C@@H]2C)ccn1.O=CO
Reaction #69592
title compound
Ausbeute 120.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)NCc3ccnc(C(=O)O)c3)cc2F)C1
Reaction #88195
(R)-4-((6-(3-(2-ethoxyphenoxy)piperidin-1-yl)-5-fluoronicotinamido)methyl)picolinic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(/C=C/c2n[nH]c3nc(-c4ccc(O)cc4)cc(C(=O)N4CCNCC4)c23)cc1)N1CCCCC1
Reaction #169225
title compound
Ausbeute 93.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)N1CCN(C(=O)c2cc(-c3ccc(O)cc3)nc3c2c(/C=C/c2ccccc2)nn3C2CCCCO2)CC1
Reaction #169235
4-[6-(4-Hydroxy-phenyl)-3-((E)-styryl)-1-(tetrahydro-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carbonyl]-piperazine-1-carboxylic acid dimethylamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(-c2ccccc2)nc(-c2ccccc2)c1)N1CCC(N2CCCC(C(=O)N3CCNCC3)C2)CC1
Reaction #190483
DOI: 10.1039/C8SC04228D
CCC(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(C=O)c1
Reaction #190963
DOI: 10.1039/C8SC04228D
CCCCc1ccc(NC2CCN(Cc3ccnc(-c4cc(OC)c(OC)c(OC)c4)c3)CC2)cc1
Reaction #229431
DOI: 10.1039/C8SC04228D
CN(C)Cc1ccnc(CSCCC(=N)NC#N)c1
Reaction #231561
DOI: 10.1039/C8SC04228D
COc1ccc(CN2Cc3c(F)c(NC(CC(C)C)C(N)=O)nc(-c4ccco4)c3C2=O)c(OC)c1
Reaction #246260
DOI: 10.1039/C8SC04228D
Cn1cc(-c2nc(NC3CCCCC3NC(=O)OC(C)(C)C)c(Br)c3c2C(=O)NC3)cn1
Reaction #246808
DOI: 10.1039/C8SC04228D
Cc1ncc(CNc2ccc(-c3ccc(C#N)cc3)cc2)c(CN(CCCCCC(=O)OCc2ccccc2)C(=O)OC(C)(C)C)c1OCc1ccccc1
Reaction #254051
DOI: 10.1039/C8SC04228D
CN(C)Cc1cc(C(=O)Nc2nc(-c3ccco3)c(C(=O)c3ccccc3)s2)ccn1
Reaction #258100
DOI: 10.1039/C8SC04228D
CCC(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(CO)c1
Reaction #260268
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCC#Cc1cc(C(=O)NCC23CC4CC(CC(C4)C2)C3)c(Cl)cn1
Reaction #264309
DOI: 10.1039/C8SC04228D
CCC(NC(=O)c1cncc2c1cnn2-c1ccc(F)cc1)c1ccnc(C(C)O)c1
Reaction #276764
DOI: 10.1039/C8SC04228D
COc1cc(-c2cc(CN3CCN(C(=O)C=Cc4ccccc4)CC3)ccn2)cc(OC)c1OC
Reaction #284482
DOI: 10.1039/C8SC04228D
O=C(Nc1nc(-c2ccco2)c(-c2ccncc2)s1)c1ccnc(Cn2ccnc2)c1
Reaction #290823
DOI: 10.1039/C8SC04228D
COc1cc(-c2cc(CN3CCC(=O)CC3)ccn2)cc(OC)c1OC
Reaction #296403
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc2nc(-c3cccc(C(F)(F)F)c3)c(CN3CCC(N4CCCCC4)CC3)c(C(=O)N[C@H](c3ccccc3)C(F)(F)F)c2c1
Reaction #332340
3-(1,4′-bipiperidin-1′-ylmethyl)-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-N-[(1R)-2,2,2-trifluoro-1-phenylethyl]-4-quinolinecarboxamide
Ausbeute 31.4%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter