#5085330

CC1(C)OB(c2ccc(NC(=O)c3cc4ccccc4o3)cc2)OC1(C)C
Reaction #57590
benzofuran-2-carboxylic acid [4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amide
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)C(NS(=O)(=O)c1ccc(-c2ccc(OC(=O)c3cc4ccccc4o3)cc2)cc1)C(=O)OC(C)(C)C
Reaction #57731
benzofuran-2-carboxylic acid 4′-(1-tert-butoxycarbonyl-2-methyl-propylsulfamoyl)-biphenyl-4-yl ester
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(Nc1ccc(-c2ccc(S(=O)(=O)O)cc2)cc1)c1cc2ccccc2o1
Reaction #57773
4′-[(benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonic acid
Ausbeute 85.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(NO)c1ccc(OCCNC(=O)c2cc3ccccc3o2)cc1
Reaction #57977
N-hydroxy-4-[2-(benzofuran-2-yl-carbonylamino)-ethoxy]-benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)c1ccc(SCCNC(=O)c2cc3ccccc3o2)cc1
Reaction #57996
methyl 4-{2-[(benzofuran-2-yl-carbonyl)-amino]ethylsulfanyl}benzoate
Ausbeute 38.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
OCc1cc2ccccc2o1
Reaction #64793
Benzofuran-2-methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
OCc1cc2ccccc2o1
Reaction #64813
Benzofuran-2-methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(NC1C2CCN(CC2)C1Cc1cccnc1)c1cc2ccccc2o1
Reaction #73561
white powder
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(N[C@@H]1C2CCN(CC2)[C@H]1Cc1cccnc1)c1cc2ccccc2o1
Reaction #73566
(2S,3R)—N-(2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-yl)benzofuran-2-carboxamide
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C1(NC(=O)c2cc3ccccc3o2)CCCCC1
Reaction #161003
title compound
Ausbeute 80.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1C2CCN(CC2)C1Cc1cccnc1)c1cc2ccccc2o1
Reaction #169606
white powder
Ausbeute 55.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1C2CCN(CC2)C1Cc1cccnc1)c1cc2ccccc2o1
Reaction #169607
white powder
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(N[C@@H]1C2CCN(CC2)[C@H]1Cc1cccnc1)c1cc2ccccc2o1
Reaction #169612
(2S,3R)—N-(2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-yl)benzofuran-2-carboxamide
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1ccc(Br)cc1)c1cc2ccccc2o1
Reaction #173469
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(-c2ccc(S(=O)(=O)O)cc2)cc1)c1cc2ccccc2o1
Reaction #186721
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCc1cc2ccccc2o1
Reaction #188447
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NCCCO)c1cc2ccccc2o1
Reaction #196098
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCC(c2c[nH]c3ccc(NC(=O)c4cc5ccccc5o4)cc23)CC1
Reaction #241458
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C(CC(C)C)NC(=O)N1CC(O)C(NC(=O)C(CC(C)C)NC(=O)c2cc3ccccc3o2)CCC1C
Reaction #243379
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1CCC(N2C(=O)c3cccc(CNC(=O)c4cc5ccccc5o4)c3C2=O)C(=O)N1
Reaction #251897
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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