1H-indole-6-carboxylic acid methyl ester

CCCCn1ccc2ccc(C(=O)OC)cc21
Reaction #42499
methyl 1-butyl-1H-indole-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc2ccn(C)c2c1
Reaction #46580
title compound
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc2ccn(CC3CCCCC3)c2c1
Reaction #179461
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc2ccn(CCOc3ccc(C=O)cc3)c2c1
Reaction #206243
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCn1ccc2ccc(C(=O)OC)cc21
Reaction #231234
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc2c(C(=O)C3C(C)(C)C3(C)C)c[nH]c2c1
Reaction #241924
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCc1ccc2cc[nH]c2c1
Reaction #244320
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc2c(C(C)=O)c[nH]c2c1
Reaction #263583
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc2ccn(Cc3ccccn3)c2c1
Reaction #270803
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc2c(C3CCCCC3)c(-c3ccc(F)cc3CNC(=O)OC(C)(C)C)[nH]c2c1
Reaction #278639
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc2ccn(C(C)C)c2c1
Reaction #285432
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc2c(Cl)c[nH]c2c1
Reaction #289809
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc2c(C3CCCCC3)c(-c3ccc(OC)cc3CO[Si](C(C)C)(C(C)C)C(C)C)[nH]c2c1
Reaction #296061
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCn1cc(C#N)c2ccc(C(=O)O)cc21
Reaction #298242
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc2c(C(=O)C3C(C)(C)C3(C)C)c[nH]c2c1
Reaction #314594
title compound
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCn1cc(C#N)c2ccc(C(=O)O)cc21
Reaction #339666
3-cyano-1-ethyl-1H-indole-6-carboxylic acid
Выход 95.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC(=O)c1ccc2c(C(=O)C(C)C)c[nH]c2c1
Reaction #365253
Methyl 3-isobutyrylindole-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
COC(=O)c1ccc2c(C(C)=O)c[nH]c2c1
Reaction #365256
Methyl 3-acetylindole-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCCCCCCCCCCC(=O)c1c[nH]c2cc(C(=O)OC)ccc12
Reaction #371948
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)c1ccc2c(C(=O)C(C)C)c[nH]c2c1
Reaction #396961
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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