N-Boc-3-pyrrolidinone

CC(C)(C)OC(=O)N1CCC(Nc2cccc(-c3ccnc(Cl)n3)c2)C1
Reaction #43023
3-[3-(2-Chloro-pyrimidin-4-yl)-phenylamino]-pyrrolidine-1-carboxylic acid tert-butyl ester
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N[C@@]1(C(=O)O)CN(C2CCNC2)C[C@@H]1CCCB(O)O
Reaction #89651
(3R,4S)-3-amino-4-(3-boronopropyl)-1,3′-bipyrrolidine-3-carboxylic acid
Ausbeute 112.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)N1CCC(O)(c2ccccc2)C1
Reaction #89699
desired product
Ausbeute 49.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1nn(-c2ccccc2)c2nc(C3CCN(C4CCN(C(=O)OC(C)(C)C)C4)CC3)[nH]c(=O)c12
Reaction #155910
tert-butyl 3-(4-(3-methyl-4-oxo-1-phenyl-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidin-6-yl)piperidin-1-yl)pyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCc1nn(-c2ccccc2)c2nc(C3CCN(C4CCNC4)CC3)nc(O)c12.Cl
Reaction #155913
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N1CCC(O)(c2ccc(F)c(Cl)c2)C1
Reaction #180795
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCC(O)(c2cccc(Cl)c2Cl)C1
Reaction #228403
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CCC(O)(c2ccc(Br)cc2)C1
Reaction #228987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C=C1CCN(C(=O)OC(C)(C)C)C1
Reaction #241425
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CCC(Nc2cccc(-c3ccnc(Cl)n3)c2)C1
Reaction #269365
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CCC(O)(c2cc(F)cc(Cl)c2)C1
Reaction #270212
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CCC(O)C1
Reaction #285939
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=C1CCN(C(=O)OC(C)(C)C)C1
Reaction #287828
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CCC(O)(c2ccc(F)c(F)c2)C1
Reaction #299584
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN(C)/C=C1/CN(C(=O)OC(C)(C)C)CC1=O
Reaction #312750
crude title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CN(C)C=C1CN(C(=O)OC(C)(C)C)CC1=O
Reaction #328730
tert-Butyl 3-[(dimethylamino)methylene]-4-oxopyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CN(C)/C=C1/CN(C(=O)OC(C)(C)C)CC1=O
Reaction #328741
tert-Butyl (3Z)-3-[(dimethylamino)methylene]-4-oxopyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(=O)C1CN(C(=O)OC(C)(C)C)CC1=O
Reaction #328745
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)N1CCC(O)(c2ccc(Cl)cc2)C1
Reaction #329728
1-t-butoxycarbonyl-3-(4-chlorophenyl)-3-hydroxypyrrolidine
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)N1CCC(O)(C(F)(F)F)C1
Reaction #357290
subtitled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
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