Teilstruktursuche

17884

CCOCc1nc2c(N)nc(C)c(C)c2n1CCC1CCN(C(=O)[C@@H]2C[C@H]2c2ccccc2)CC1
Reaction #11468
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(N)c2nc(C)n(CCCNC(=O)[C@@H]3C[C@H]3c3ccccc3)c2c1C
Reaction #11469
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(=O)C2CC2c2ccccc2)sc1C(=O)NCc1ccccc1
Reaction #73609
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C1CC1c1cc(F)c(OCc2ccccc2)c(F)c1
Reaction #91180
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC[C@@H](Cc2ccccc2)N1C(=O)C1CC1c1cc(F)c(OCc2ccccc2)c(F)c1
Reaction #91181
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CC2C(=O)Cl)cc1F
Reaction #91186
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CC2C(=O)N2C(=O)OC[C@H]2Cc2ccccc2)cc1F
Reaction #91187
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C1CC1c1ccccc1)N1CCN(C2CC2)CC1
Reaction #195378
DOI: 10.1039/C8SC04228D
CCOCc1nc2c(N)nc(C)c(C)c2n1CCC1CCN(C(=O)C2CC2c2ccccc2)CC1
Reaction #266596
DOI: 10.1039/C8SC04228D
O=C(C1CC1c1ccccc1)N1CCN(C2CCCCCC2)CC1
Reaction #282147
DOI: 10.1039/C8SC04228D
CCOC(=O)CC(=O)C1CC1c1ccccc1
Reaction #318305
ethyl 3-(2-phenyl-1-cyclopropyl)-3-oxo-propanoate
Ausbeute 108.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C1CC1c1ccccc1)N1CCN(C2CCCC2)CC1
Reaction #388040
DOI: 10.1039/C8SC04228D
COc1cc(-c2nn(C3CCN(C)CC3)c3ncnc(N)c23)ccc1NC(=O)C1CC1c1ccccc1
Reaction #391983
DOI: 10.1039/C8SC04228D
CC(C)(C)N1CCN(C(=O)C2CC2c2ccccc2)CC1
Reaction #395489
DOI: 10.1039/C8SC04228D
Nc1nc2ccccc2c2c1ncn2CCCCNC(=O)[C@@H]1C[C@H]1c1ccccc1
Reaction #441035
N1-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-(trans)-2-phenylcyclopropane-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C(=O)Cl)C1c1ccc(OC(F)(F)F)c(Br)c1
Reaction #458233
3-(3-bromo-4-trifluoromethoxyphenyl)-2,2-dimethyl-cyclopropanecarboxylic acid-chloride
Ausbeute 93.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nn([C@H]3CC[C@H](N4CCN(C)CC4)CC3)c3ncnc(N)c23)ccc1NC(=O)[C@H]1C[C@@H]1c1ccccc1
Reaction #519584
trans-N1-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-2-methoxyphenyl)-(1S,2S)-2-phenylcyclopropane-1-carboxamide
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nn(C3CCN(C4CCN(C)CC4)CC3)c3ncnc(N)c23)ccc1NC(=O)[C@@H]1C[C@H]1c1ccccc1
Reaction #519601
N1-{4-[4-amino-1-[1-(1-methylpiperidin-4-yl)piperidin-4-yl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}-trans-2-phenylcyclopropane-1-carboxamide
Ausbeute 60.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nn(C3CCC(N4CCN(C)CC4)CC3)c3ncnc(N)c23)c(F)cc1NC(=O)[C@@H]1C[C@H]1c1ccccc1
Reaction #519647
trans-N1-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluoro-2-methoxyphenyl)-2-phenyl-1-cyclopropanecarboxamide
Ausbeute 88.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nn(C3CCC(N4CCN(C)CC4)CC3)c3ncnc(N)c23)c(F)cc1NC(=O)[C@@H]1C[C@H]1c1ccccc1
Reaction #519673
trans-N1-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-5-fluoro-2-methoxyphenyl)-2-phenyl-1-cyclopropanecarboxamide
Ausbeute 88.3%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter