(4-fluorophenyl)methanamine

Fc1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1
Reaction #631
Ausbeute 60.0%750 AstraZeneca ELN dataset
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1NCc1ccc(F)cc1
Reaction #7515
title compound
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Fc1ccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #8741
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Fc1ccc(CNCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #8754
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N1C(NCc2ccc(F)cc2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47011
product 85
Ausbeute 41.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1C(NCc2ccc(F)cc2)=N[C@@H]2CCCC[C@@H]21
Reaction #47026
product 193
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2cc(C(=O)O)ccc2c1CNCc1ccc(F)cc1
Reaction #51508
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1c(CO)sc2c(O)c(C(=O)NCc3ccc(F)cc3)cnc12
Reaction #51908
title compound
Ausbeute 85.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(NCc1ccc(F)cc1)c1ccncc1Nc1ccc(I)cc1F
Reaction #67872
N-(4-Fluoro-benzyl)-3-(2-fluoro-4-iodo-phenylamino)-isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1ccc2c(C(=O)NCc3ccc(F)cc3)c(C(C)C)n(Cc3ccccn3)c2c1
Reaction #68352
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Fc1ccc(CNc2ccc3nc[nH]c3c2)cc1
Reaction #74209
N-(4-Fluorobenzyl)-3H-benzo[d]imidazol-5-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
—
Reaction #75963
oil
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cc2c(cc1OC)C(Cc1ccccc1)N(CC(=O)NCc1ccc(F)cc1)CC2
Reaction #76882
2-(1-Benzyl-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-N-(4-fluoro-benzyl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(CC2c3cc(OC)c(OC)cc3CCN2CC(=O)NCc2ccc(F)cc2)cc1OC
Reaction #76906
2-[1-(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(4-fluoro-benzyl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C1Cc2cc(S(=O)(=O)NCc3ccc(F)cc3)ccc2N1
Reaction #77389
2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid-4-fluoro-benzylamide
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(NCc1ccc(F)cc1)c1cnc2cc(NC(=O)c3ccccc3-c3ccc(C(F)(F)F)cc3)ccc2c1
Reaction #80221
title compound
Ausbeute 76.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1n[nH]c(N)c1-c1nc2ccc(S(=O)(=O)NCc3ccc(F)cc3)cc2s1
Reaction #85528
title compound
Ausbeute 9.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccncc1NCc1ccc(F)cc1
Reaction #91312
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccncc1NCc1ccc(F)cc1
Reaction #91313
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1nc(NCc2ccc(F)cc2)nc(NC2CCCCC2)c1C
Reaction #91378
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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