4-aminobutan-1-ol

NCCCCOc1cccc2nccn12
Reaction #5526
desired product
収率 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=[N+]([O-])c1cnc2cc(Br)ccc2c1NCCCCO
Reaction #9511
4-(7-bromo-3-nitroquinolin-4-ylamino)butan-1-ol
収率 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc2c(c1)c(CC(=O)NCCCCO)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #44939
N-(4-hydroxybutyl)-2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetamide
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)[Si](C)(C)OCCCCNCCOCc1ccccc1
Reaction #46289
silyloxybutyl-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)CNCCCCO
Reaction #46295
tert-Butyl[(4-hydroxybutyl)amino]acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)Cc1ccc(COCCCCN)o1
Reaction #63322
title compound
収率 29.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CC(C)(C#N)NCCCCO
Reaction #64223
propanonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(NCCCCO)c1ccncc1Nc1ccc(I)cc1F
Reaction #67822
3-[(2-fluoro-4-iodophenyl)amino]-N-(4-hydroxybutyl)isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCOCCCCNS(=O)(=O)c1ccccc1
Reaction #69072
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCOCCCCNS(=O)(=O)c1cccc(OCC2CC2)c1
Reaction #69073
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1nc[nH]c1CSCCN=C(NC#N)NCCCCO
Reaction #96192
title compound
収率 38.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COC(=O)c1ccc(C(=O)NCCCCO)cc1
Reaction #155828
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NCCCCO)c1ccncc1Nc1ccc(I)cc1F
Reaction #165987
3-[(2-fluoro-4-iodophenyl)amino]-N-(4-hydroxybutyl)isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NCCCCO)cn1
Reaction #170518
title compound
収率 37.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1C2CC3CC(C2)CC1C3)c1cnn(-c2ccccc2)c1NCCCCO
Reaction #180092
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2ccccc2C(=O)N1CCCCO
Reaction #183900
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C)cc(NCCCCO)c1
Reaction #186072
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NCCCCO)cn1
Reaction #186361
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
—
Reaction #214913
( b )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
COc1cc(C(=O)NCCCCO)ccc1Nc1ncc2c(n1)N(C1CCCC1)CC(F)(F)C(=O)N2C
Reaction #239558
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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