5-formylindole

O=[N+]([O-])C=Cc1ccc2[nH]ccc2c1
Reaction #43201
5-(2-nitro-vinyl)-1H-indole
المردود 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1ccc(Cn2nnnc2C(NCCCn2ccnc2)c2ccc3[nH]ccc3c2)cc1
Reaction #46741
[[1-(4-Chloro-benzyl)-1H-tetrazol-5-yl]-(1H-indol-5-yl)-methyl]-(3-imidazol-1-yl-propyl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCN(Cc2ccc3[nH]ccc3c2)CC1
Reaction #49253
5-[4-(tert-butoxycarbonyl)piperazin-1-ylmethyl]indole
المردود 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
OCCN1CCN(Cc2ccc3[nH]ccc3c2)CC1
Reaction #49256
5-[4-(2-hydroxyethyl)piperazin-1-ylmethyl]indole
المردود 132.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)Cc1ccc2c(ccn2C(=O)OC(C)(C)C)c1
Reaction #49267
5-(dimethylaminomethyl)-1-(tert-butoxycarbonyl)indole
المردود 36.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1ccc2cc(C=O)ccc21
Reaction #68860
title compound
المردود 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NS(=O)(=O)c1ccc2c(c1)C(=Cc1ccc3[nH]ccc3c1)C(=O)N2
Reaction #77377
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CNS(=O)(=O)c1ccc2c(c1)C(=Cc1ccc3[nH]ccc3c1)C(=O)N2
Reaction #77380
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CN(C)S(=O)(=O)c1ccc2c(c1)C(=Cc1ccc3[nH]ccc3c1)C(=O)N2
Reaction #77384
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O[C@@H]1C[C@@H](C(c2ccccc2)c2ccccc2)OC[C@H]1NCc1ccc2[nH]ccc2c1
Reaction #166125
(2S,4R,5R)-2-benzhydryl-5-[(1H-indol-5-ylmethyl)-amino]-tetrahydropyran-4-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O[C@H]1C[C@H](C(c2ccccc2)c2ccccc2)OC[C@@H]1NCc1ccc2[nH]ccc2c1
Reaction #166127
(2R,4S,5S)-2-benzhydryl-5-[(1H-indol-5-ylmethyl)-amino]-tetrahydropyran-4-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(C(Cc1ccccc1)NCc1ccc2[nH]ccc2c1)N1CCN(Cc2ccccc2)CC1
Reaction #182400
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=[N+]([O-])C=Cc1ccc2[nH]ccc2c1
Reaction #196953
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1ccc2cc(C=O)ccc21
Reaction #210206
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1ccc2cc(C=O)ccc21
Reaction #212113
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(S(=O)(=O)n2ccc3cc(C=O)ccc32)cc1
Reaction #212317
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])C=Cc1ccc2[nH]ccc2c1
Reaction #216153
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(C)C(=O)Nc1cccc(C2CCN(Cc3ccc4[nH]ccc4c3)CC2)c1
Reaction #225750
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CNS(=O)(=O)c1ccc2c(c1)C(=Cc1ccc3[nH]ccc3c1)C(=O)N2
Reaction #239122
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
الصفحة 1التالي