indomethacin

COc1ccc2c(c1)c(CC(=O)NCCCCN)c(C)n2C(=O)c1ccc(Cl)cc1.Cl
Reaction #44936
N-(4-aminobutyl)-2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetamide hydrochloride
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(c1)c(CC(=O)NCCNC(=O)OC(C)(C)C)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #44937
tert-Butyl 2-[2-{1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl}acetamido]ethylcarbamate
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(c1)c(CC(=O)NCCCNC(=O)OC(C)(C)C)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #44938
tert-Butyl 3-[2-{1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl}acetamido]propylcarbamate
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(c1)c(CC(=O)NCCCCO)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #44939
N-(4-hydroxybutyl)-2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetamide
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(c1)c(CC(=O)N(c1nccs1)C1CCCCC1)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #252363
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc2c(c1)c(CC(=O)O)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #276678
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc2c(c1)c(CC(=O)OCc1cccnc1)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #348632
1-(p-chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid-3 -pyridylmethyl ester
Выход 79.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_08
CCOCOC(=O)Cc1c(C)n(C(=O)c2ccc(Cl)cc2)c2ccc(OC)cc12
Reaction #348633
1-(p-chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid-ethoxymethyl ester
Выход 71.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_08
COc1ccc2c(c1)c(CC(=O)O)c(C)n2C(=O)c1ccc(Cl)cc1.NCC(=O)O
Reaction #363326
title product
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCOCOC(=O)Cc1c(C)n(C(=O)c2ccc(Cl)cc2)c2ccc(OC)cc12
Reaction #397021
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc2c(c1)c(CC(=O)OCCNC(=O)c1cccnc1)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #399427
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
NCCc1c[nH]c2ccc(O)cc12
Reaction #414258
serotonin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
COc1ccc2c(c1)c(CC(=O)OSCc1ccccn1)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #445218
1-(p-chlorobenzoyl)-5-methoxy-2-methyl-3-indol acetic acid-2-pyridylmethylthioester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_08
COc1ccc2c(c1)c(CC(=O)OCCNC(=O)c1cccnc1)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #447066
N-(2-{[1-(p-Chlorobenzoyl)- 5-methoxy-2-methyl-3-indolyl]acetoxy}ethyl)-3-pyridinecarboxamide
Выход 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #466271
dicyclohexyl urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
COc1ccc2c(c1)c(CC(=O)OCC(=O)OC(C)(C)C)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #502133
title compound
Выход 99.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COc1ccc2c(c1)c(CC(=O)O)c(CBr)n2C(=O)c1ccc(Cl)cc1
Reaction #535350
(2-(Bromomethyl)-1-(4-chlorobenzoyl)-5-methoxy-1H-indol-3-yl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1ccc2c(c1)c(CCO)c(C)n2Cc1ccc(Cl)cc1
Reaction #567259
title compound
Выход 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
COc1ccc2c(c1)c(CC(=O)O)c(C)n2C(=O)c1ccc(Cl)cc1.NCC(=O)O
Reaction #569197
title product
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
COc1ccc2c(c1)c(CC(=O)NCCCCN)c(C)n2C(=O)c1ccc(Cl)cc1.Cl
Reaction #624847
N-(4-aminobutyl)-2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetamide hydrochloride
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
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