furan-2-carboxylic acid

COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)c2ccco2)c1
Reaction #41374
N-((1R,2S)-1-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-1-(3-methoxyphenyl)propan-2-yl)furan-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(N[C@@H](Cc1c[nH]c2ccccc12)c1nc(-c2ccccc2)c[nH]1)c1ccco1
Reaction #51644
expected product
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(Nc1cc(F)c2c(c1)c(/C=C/c1cccnc1)nn2C(=O)c1ccco1)c1ccco1
Reaction #62307
title compound
収率 37.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(NC/C=C\COc1cc(CN2CCCCC2)ccn1)c1ccco1
Reaction #80342
title compound
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(ON1C(=O)CCC1=O)c1ccco1
Reaction #176571
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccco1)N1CCN(c2nc(N3CCS(=O)CC3)c3ncnc(SCCc4ccccc4)c3n2)CC1
Reaction #201650
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NCc1cc(NC2CCCC2)c2[nH]c(C3=NC(CO)CS3)cc2c1)c1ccco1
Reaction #234497
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NCC(=O)N1CCN(C(=O)c2ccco2)CC1)c1ccc(Oc2ccccc2)cc1
Reaction #248768
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)CCC(NC(=O)c1ccc(-c2ccc(NC(=O)c3ccco3)cc2)cc1)C(=O)OC(C)(C)C
Reaction #272027
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)NC(=O)c1ccco1
Reaction #281955
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)NC1=NC(C)(c2cccc(NC(=O)c3ccco3)c2)COC1
Reaction #308850
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)NC(=O)c1ccco1
Reaction #315004
N-tert-butylfuran-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCCN1C[C@H](O)[C@@H](NC(=O)[C@H](CC2CCCCC2)NC(=O)c2ccco2)CC[C@H]1C
Reaction #317014
title compound
収率 76.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C(N[C@@H](Cc1c[nH]c2ccccc12)c1nc(-c2ccccc2)c[nH]1)c1ccco1
Reaction #317559
expected product
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1ccc2ccc(NC(=O)c3ccco3)nc2n1
Reaction #323040
N-(7-Methoxy-1,8-naphthyridin-2-yl)-2-furancarboxamide
収率 83.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
O=C(Nc1ccc2ccc(Oc3ccccc3)nc2n1)c1ccco1
Reaction #323041
N-(7-Phenoxy-1,8-naphthyridin-2-yl)-2-furancarboxamide
収率 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
Cc1ccc(-c2occc2C(N)=O)cc1
Reaction #361289
white crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
Cc1ccc(-c2occc2C(N)=O)cc1
Reaction #361433
white crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
—
Reaction #367903
methoxy carboxylic acids
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
O=C(Nc1cnc(OCC(F)(F)F)c(-c2ccc(Cl)cc2)c1)c1ccco1
Reaction #379560
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
1 ページ次のページ