#11205967

Cn1cc(C(=O)O)c2ccccc21
Reaction #5463
colorless crystals
収率 75.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(NCC12CCCN(CCC1)C2)c1c[nH]c2ccccc12
Reaction #5476
title compound
収率 57.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(OCC12CCCN(CC1)C2)c1c[nH]c2ccccc12
Reaction #5479
colorless solid
収率 52.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(OCC12CCCN(CCC1)C2)c1c[nH]c2ccccc12
Reaction #5482
colorless crystals
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)CN1C2CC(OC(=O)c3c[nH]c4ccccc34)CC1CC(C(=O)OC)C2
Reaction #48480
7-(1H-Indole-3-carbonyloxy)-9-methoxycarbonylmethyl-9-aza-bicyclo[3.3.1]nonane-3-carboxylic acid methyl ester
収率 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1c[nH]c2cc(Br)ccc12
Reaction #51691
6-bromoindole-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCCCn1cc(C(=O)O)c2ccccc21
Reaction #84207
title compound
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Cl)c1c[nH]c2ccccc12
Reaction #90240
indole-3-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(c1c[nH]c2ccccc12)N1CCCC2c3ccccc3CC21
Reaction #173790
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[N-]=[N+]=NC(=O)c1c[nH]c2ccccc12
Reaction #174069
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(NC(=O)c1c[nH]c2ccccc12)c1ccccn1
Reaction #189647
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1cn(S(=O)(=O)c2ccccc2)c2ccccc12
Reaction #203715
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1c[nH]c2ccccc12
Reaction #216175
compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCCCn1cc(C(=O)O)c2ccccc21
Reaction #216747
1-butylindole-3-carboxylic acid
収率 86.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COc1ccc(S(=O)(=O)n2cc(C(=O)O)c3ccccc32)c2ccccc12
Reaction #244036
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN1CCN(C(=O)c2c[nH]c3ccccc23)CC1
Reaction #341372
(1H-Indol-3-yl)-(4-methylpiperazin-1-yl)methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCCCCCCCCOC(=O)c1c[nH]c2ccccc12
Reaction #348014
nonyl indole-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
O=C(N[C@H]1CCN(C(=O)c2cc(Cl)cc(Cl)c2)[C@H](Cc2ccccc2)C1)c1c[nH]c2ccccc12
Reaction #351875
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCCn1cc(C(=O)O)c2ccccc21
Reaction #371412
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cn1cc(C(=O)O)c2ccccc21
Reaction #378191
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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