thiophene-2-carboxylic acid

COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)c2cccs2)c1
Reaction #41375
N-((1R,2S)-1-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-1-(3-methoxyphenyl)propan-2-yl)thiophene-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCc1nc2c(n1Cc1ccc(-c3ccccc3-c3nnn[nH]3)cc1)C(C(=O)OC)N(C(=O)c1cccs1)CC2
Reaction #50135
methyl 2-n-butyl-5-(2-thienyl)carbonyl-3-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate
Rendimiento 51.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=C(NC/C=C\COc1cc(CN2CCCCC2)ccn1)c1cccs1
Reaction #80337
title compound
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)c1ccc(CCCBr)s1
Reaction #87964
title compound
Rendimiento 123.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CS(=O)(=O)c1ccc(-c2nc(C(F)(F)F)nc(N3CCN(C(=O)c4cccs4)CC3)c2-c2ccccc2)cc1
Reaction #159851
title compound
Rendimiento 48.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cl
Reaction #177309
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1cccs1)N1CCNCC1
Reaction #178279
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1cc([N+](=O)[O-])cs1
Reaction #196464
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(CNC(=O)c1cccs1)NC(=O)c1sc(C(=O)NCc2cccc3[nH]ncc23)cc1C(F)(F)F
Reaction #199006
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[C-]#N
Reaction #205223
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)c1cccs1
Reaction #205278
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(C(=O)O)s1
Reaction #208282
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1ccc(C(=O)O)s1
Reaction #216436
desired acid 35
Rendimiento 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CN(Cc1cccc(-c2ccc(CC3SC(=O)NC3=O)cc2)c1)C(=O)c1cccs1
Reaction #222967
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NC(CNC(=O)c1cccs1)C(=O)O)OCC1c2ccccc2-c2ccccc21
Reaction #224787
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCN(CC(O)(CNc1cccc2c1cnn2-c1ccc(F)cc1)C(F)(F)F)C(=O)c1cccs1
Reaction #250024
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NCC(F)(F)F)c1cccs1
Reaction #258799
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)c1ccc(C(O)c2cccc(C=Cc3ccc4ccc(Cl)cc4n3)c2)s1
Reaction #261925
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1cccs1)c1cccs1
Reaction #270013
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCN(CC(O)(CNc1cccc2c1cnn2-c1ccccc1)C(F)(F)F)C(=O)c1cccs1
Reaction #273650
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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