β-alanine

CC(C)C(=O)C(=Cc1ccccc1)C(=O)Nc1ccccc1
Reaction #5780
4-methyl-3-oxo-N-phenyl-2-(phenylmethylene)pentanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)C(=O)C(=Cc1ccccc1)C(=O)Nc1ccccc1
Reaction #5786
4-methyl-3-oxo-N-phenyl-2-(phenylmethylene)pentanamide
Ausbeute 84.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cccc(C=C2NC(=O)NC2=O)c1OCc1ccccc1
Reaction #5992
5-[[3-Methoxy-2-(phenylmethoxy)phenyl]methylene]-2,4-imidazolidinedione
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(Cc1ccccc1)NCCC(=O)O
Reaction #6534
N-carboxyethyl-amphetamine
Ausbeute 60.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)NCCC(=O)O
Reaction #40286
N-Acetyl-β-alanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CSC(=S)NCCC(=O)O
Reaction #55406
methyl 2-carboxyethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(O)CCNc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #82439
solid
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C1CCNC2=COc3ccc(Nc4nc(Nc5cccc(O)c5)ncc4F)cc3N12
Reaction #158814
5-fluoro-N2-(3-hydroxyphenyl)-N4-[1-oxo-1,2,3,6-tetrahydropyrimido[2,1-c][1,4]benzoxazin-9-yl]-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1CCNC2=COc3ccc(Nc4nc(Nc5cccc(O)c5)ncc4F)cc3N12
Reaction #163925
5-fluoro-N2-(3-hydroxyphenyl)-N4-[1-oxo-1,2,3,6-tetrahydropyrimido[2,1-c][1,4]benzoxazin-9-yl]-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CON1C(C)(C)CC(CCCCNc2nc(NCCCCC3CC(C)(C)N(OC)C(C)(C)C3)nc(NCCC(=O)O)n2)CC1(C)C
Reaction #181343
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC(=Cc1ccc2[nH]ccc2c1)C(=O)c1ccc(O)c(O)c1
Reaction #182977
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1NC(=O)C(=Cc2ccc(N3CCC4(CC3)OCCO4)c(F)c2)S1
Reaction #185635
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(=O)C(=Cc1ccccc1)C(=O)Nc1ccccc1
Reaction #191163
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCN1C(=O)c2ccccc2C1=O
Reaction #192132
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C=C2SC(=S)NC2=O)cc(CN(C)C)c1O
Reaction #197784
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCNc1cc(Oc2ccc(Cl)cc2Cl)ccc1[N+](=O)[O-]
Reaction #204359
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCON1C(C)(C)CC(CCCCNc2nc(NCCCCC3CC(C)(C)N(OCCCCCCCC)C(C)(C)C3)nc(NCCC(=O)O)n2)CC1(C)C
Reaction #205531
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C=C2SC(=S)NC2=O)cc(CN(C)C)c1O
Reaction #215910
product
Ausbeute 74.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COc1cc(C=C2NC(=O)NC2=O)ccc1O
Reaction #215917
product
Ausbeute 42.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COc1cc(C=C2C(=O)NC(=O)N2C)ccc1O
Reaction #215925
product
Ausbeute 14.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
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