1H-indazole-3-carboxylic acid

CON(C)C(=O)c1n[nH]c2ccccc12
Reaction #156100
N-methoxy-N-methyl-1H-indazole-3-carboxamide
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1n[nH]c2ccccc12
Reaction #198905
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C)c(S(=O)(=O)n2nc(C(=O)O)c3ccccc32)c(C)c1
Reaction #203347
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1n[nH]c2ccc([N+](=O)[O-])cc12
Reaction #224817
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1n[nH]c2ccccc12
Reaction #298950
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CON(C)C(=O)c1n[nH]c2ccccc12
Reaction #305640
N-methoxy-N-methyl-1H-indazole-3-carboxamide
Ausbeute 81.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CN(C)C(=O)c1n[nH]c2ccccc12
Reaction #327980
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C(Nc1ccc(N2CCCC2=O)cc1)c1n[nH]c2ccccc12
Reaction #388709
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(NCCN1CCOCC1)c1n[nH]c2ccccc12
Reaction #393490
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(OCc1ccccc1)c1nn(Cc2ccccc2)c2ccccc12
Reaction #430276
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
Cc1cccc(CN2CCN(C)CC(NC(=O)c3n[nH]c4ccccc34)C2)c1
Reaction #461283
title compound
Ausbeute 32.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
Cc1ccc(C)c(CN2CCN(C)CC(NC(=O)c3n[nH]c4ccccc34)C2)c1
Reaction #461284
title compound
Ausbeute 67.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
CN1CCN(Cc2ccccc2)CC(NC(=O)c2n[nH]c3ccccc23)C1
Reaction #461286
title compound
Ausbeute 54.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
CC1CN(Cc2ccccc2)CC(NC(=O)c2n[nH]c3ccccc23)CN1C
Reaction #461290
title compound
Ausbeute 18.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
CN1CCN(C)CC(OC(=O)c2n[nH]c3ccccc23)C1
Reaction #461291
title compound
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
O=C(NCCCCN1CCCCC1)c1n[nH]c2ccccc12
Reaction #486230
oil
Ausbeute 101.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
O=C(NCCN1CCOCC1)c1n[nH]c2ccccc12
Reaction #486231
colorless crystals
Ausbeute 24.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
O=C(NCCN1CCc2ccccc2C1)c1n[nH]c2ccccc12
Reaction #486232
solid
Ausbeute 185.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CON(C)C(=O)c1n[nH]c2ccccc12
Reaction #502106
compound
Ausbeute 69.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
O=C(NCCCCN1CCCCC1)c1n[nH]c2ccccc12
Reaction #569763
oil
Ausbeute 101.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
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