3-(Boc-amino)-1-propanol

CC(C)(C)OC(=O)NCCCOc1cccc2c(Cl)nccc12
Reaction #10597
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)NCCCON1Cc2cccc(-c3cc4cc(CN5CCCCC5)ccc4n3C(=O)OC(C)(C)C)c2C1=O
Reaction #49377
(3-(tert-butoxycarbonylamino)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)NCCCOc1ccc(-c2cc3cc(C=O)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49399
4-[3-(tert-butoxycarbonylamino)propoxy]-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone
Yield 99.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)NCCC=O
Reaction #66331
N-Boc-3-amino-propanal
Yield 86.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)NCCC=O
Reaction #66398
N-Boc-3-amino-propanal
Yield 86.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)NCCC=O
Reaction #155399
N-Boc-3-amino-propanal
Yield 86.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(-c2cn(S(=O)(=O)c3ccccc3)c3ncccc23)nc(NCc2cccc(OCCCNC(=O)OC(C)(C)C)c2)n1
Reaction #155527
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)NCCCOS(C)(=O)=O
Reaction #176834
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)OCC1OC(O)(CCCNC(=O)OC(C)(C)C)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #189579
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NCCCOc1cc(F)ccc1F
Reaction #230023
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCSc1ccc(C(=O)OC)c(OCCCNC(=O)OC(C)(C)C)c1
Reaction #233225
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cccc(OCCCNC(=O)OC(C)(C)C)c1-c1cc(Nc2cnc(C#N)cn2)n[nH]1
Reaction #241396
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)C(F)(F)F
Reaction #315275
TFA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)(C)OC(=O)NCCC=O
Reaction #328966
N-Boc-3-amino-propanal
Yield 86.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)NCCCOc1c(F)ccc([N+](=O)[O-])c1F
Reaction #330408
title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)NCCC=O
Reaction #331672
N-Boc-3-amino-propanal
Yield 86.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)NCCCOc1cccc2c(Cl)nccc12
Reaction #374541
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)OC(=O)NCCC=O
Reaction #378203
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccc(S(=O)(=O)OCCCNC(=O)OC(C)(C)C)cc1
Reaction #388857
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CN(C(=O)OCc1ccccc1)n1c(C(=O)OCCCNC(=O)OC(C)(C)C)c(-c2ccccc2)c2cc(Cl)ccc2c1=O
Reaction #393375
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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