1-(3-aminophenyl)ethanone

CC(=O)c1cccc(Nc2cc(C)nc(N)n2)c1
Reaction #3490
4-(3-acetylphenyl)amino-2-amino-6-methylpyrimidine
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)c1cccc(NC(=O)CN(C)C)c1
Reaction #58888
product
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
NC1=c2ccoc2=NCN1c1cccc(N)c1
Reaction #60755
4-Amino-3-(3-aminophenyl)furo[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)c1cccc(NC(=O)CC2CCc3cc(Br)cc4[nH]c(=O)c(=O)n2c34)c1
Reaction #80790
title compound
Ausbeute 87.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)c1cccc(Nc2cc(C)nc(N)n2)c1
Reaction #81893
4-(3-acetylphenyl)amino-2-amino-6-methylpyrimidine
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)c1cccc(NC(=O)C(F)(F)F)c1
Reaction #189335
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1cccc(Nc2cc(C)nc(N)n2)c1
Reaction #207593
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1cccc(NC(=O)CC2CCc3cc(Br)cc4[nH]c(=O)c(=O)n2c34)c1
Reaction #262150
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)c1cccc(Nc2nncc3c(I)c(C)ccc23)c1
Reaction #297287
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)c1cccc(NC(=O)C(F)(F)F)c1
Reaction #317888
3-acetyl-trifluoroacetylaminobenzene
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(=O)c1cccc(N=P(c2ccccc2)(c2ccccc2)c2ccccc2)c1
Reaction #323833
title compound
Ausbeute 70.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CC(=O)c1cccc(Nc2cc(C)nc3ccc4nc[nH]c4c23)c1.CC(=O)c1cccc(Nc2cc(C)nc3ccc4nc[nH]c4c23)c1.Cl.Cl.O
Reaction #355449
9-(m-Acetylanilino)-7-methyl-1H-imidazo[4,5-f]quinoline Hydrochloride Hemihydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
CC(=O)c1cccc(NC(=O)C2CCC2)c1
Reaction #392523
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)c1cccc(NC=O)c1
Reaction #404322
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)c1cccc(NC(=O)CCCC(=O)Nc2cccc(C(C)=O)c2)c1
Reaction #430023
N,N'-bis(3-acetylphenyl)pentanediamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC(=O)c1cccc(Nc2cc(C)nc(N)n2)c1
Reaction #444679
4-(3-acetylphenyl)amino-2-amino-6-methylpyrimidine
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CC(=O)c1cccc(NC(=O)CCCC(=O)Nc2cccc(C(C)=O)c2)c1
Reaction #464214
N,N'-bis(3-acetylphenyl)pentanediamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CC(=O)c1cccc(Nc2cc(C)nc(N)n2)c1
Reaction #466133
4-(3-acetylphenyl)amino-2-amino-6-methylpyrimidine
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CSC(=C[N+](=O)[O-])Nc1cccc(C(C)=O)c1
Reaction #482556
yellow powder
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCOC(=O)c1cc(C)n(-c2cccc(C(C)=O)c2)c1-c1ccccc1
Reaction #501073
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
Seite 1Weiter