2-phenylpyrrolidine

c1ccc(C2CCCN2c2ccccc2)cc1
Reaction #714
Ausbeute 90.2%750 AstraZeneca ELN dataset
COC(=O)c1cc(Cl)cnc1N1CCCC1c1ccccc1
Reaction #159618
title compound
Ausbeute 90.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1CCc2cc(/C=C/C(=O)N3CCCC3c3ccccc3)cnc2N1
Reaction #170100
title compound
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(c1cc2ccccc2n1Cc1ccc(Cl)cc1)N1CCC(C(=O)N2CCCC2c2ccccc2)CC1
Reaction #170853
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cl.NC(=O)c1ccc(Oc2ccc(CN3CCCC3c3ccccc3)cc2)nc1
Reaction #217947
title compound
Ausbeute 3.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CNC(=O)c1c(-c2ccc(F)cc2)oc2ccc(-c3cccc(C(=O)N4CCCC4c4ccccc4)c3)cc12
Reaction #259987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl.NC(=O)c1ccc(Oc2ccc(CN3CCCC3c3ccccc3)cc2)nc1
Reaction #315405
title compound
Ausbeute 3.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C(Cc1ccc(-n2nc(C(F)(F)F)c3c2CCCC3)cc1)N1CCCC1c1ccccc1
Reaction #317876
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1ccc(S(=O)(=O)N2CCCC2c2ccccc2)cc1
Reaction #394640
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cl.NC(=O)c1ccc(Oc2ccc(CN3CCCC3c3ccccc3)cc2)nc1
Reaction #579560
title compound
Ausbeute 3.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C(N1CCCC1c1ccccc1)C1(c2ccc(Cl)cc2)CC1
Reaction #591453
1-{[1-(4-chlorophenyl)cyclopropyl]carbonyl}-2-phenylpyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
Cc1nnc2ccc(N3CCCC3c3ccccc3)nn12
Reaction #608762
3-methyl-6-(2-phenylpyrrolidin-1-yl)-[1,2,4]triazolo[4,3-b]pyridazine
Ausbeute 12.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CNC(=O)c1c(-c2ccc(F)cc2)oc2ccc(-c3cccc(C(=O)N4CCCC4c4ccccc4)c3)cc12
Reaction #642275
title compound
Ausbeute 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=C(N1CCCC1c1ccccc1)C1(c2ccc(Cl)cc2)CC1
Reaction #644987
1-{[1-(4-chlorophenyl)cyclopropyl]carbonyl}-2-phenylpyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CCCC5c5ccccc5)c4)cc23)CC1
Reaction #649255
title compound
Ausbeute 22.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CCCC5CN5CCCCC5)c4)cc23)CC1
Reaction #649256
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CC[C@H](N(C)C)C5)c4)cc23)CC1
Reaction #649257
title compound
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
NS(=O)(=O)Cc1cccc(Nc2ncnc(N3CCCC3c3ccccc3)n2)c1
Reaction #674348
rac-3-[(4-(2-Phenylpyrrolidin-1-yl)-1,3,5-triazin-2-yl)amino]-benzenemethanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
O=C1CCc2cc(/C=C/C(=O)N3CCCC3c3ccccc3)cnc2N1
Reaction #721056
title compound
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
Clc1cccc(-n2nnnc2N2CCCC2c2ccccc2)c1Cl
Reaction #732834
title compound
Ausbeute 20.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
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