O-benzylhydroxylamine

COc1c(NOCc2ccccc2)ccnc1C
Reaction #1096
4-(O-Benzylhydroxylamino)-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(NC2CCC(=NOCc3ccccc3)CC2)ccnc1C
Reaction #1102
4-[4-(O-Benzyloximino)cyclohexylamino]-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1nccc(NOCc2ccccc2)c1Cl
Reaction #1114
4-(O-Benzylhydroxylamino)-3-chloro-2-ethylpyridine
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #1914
pure product
収率 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=CNc1nc(Cl)c(NC=O)c(NOCc2ccccc2)n1
Reaction #6349
title compound
収率 46.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(NOCc1ccccc1)c1cc2ccccc2s1
Reaction #65793
2-(1-(benzyloxyamino)ethyl)benzo[b]thiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(NOCc1ccccc1)c1ccncc1Nc1ccc(I)cc1F
Reaction #67862
N-(benzyloxy)-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(NOCc1ccccc1)c1ccncc1Nc1ccc(I)cc1F
Reaction #166027
N-(benzyloxy)-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=CNOCc1ccccc1
Reaction #173734
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CC(=O)NOCc1ccccc1
Reaction #187529
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(NOCc1ccccc1)c1cc2ccccc2s1
Reaction #188524
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C(CCc1nc(-c2ccccc2)c(-c2ccccc2)o1)=NOCc1ccccc1
Reaction #188962
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(OCC1OC(n2cnc3c(NOCc4ccccc4)nc(Cl)nc32)C(OC(=O)c2ccccc2)C1OC(=O)c1ccccc1)c1ccccc1
Reaction #190185
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CNOCc1ccccc1
Reaction #190344
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=S(=O)(CCCCl)NOCc1ccccc1
Reaction #191280
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)C(=NOCc1ccccc1)c1csc2ccccc12
Reaction #192304
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCCCCCCCCNC(=O)NOCc1ccccc1
Reaction #193341
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1cncc1C(O)(c1ccc(Cl)cc1)c1ccc2c(c1)c(-c1cccc(C=NOCc3ccccc3)c1)cc(=O)n2C
Reaction #193729
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCC(C(=O)N(c2cc(C3=CCC(=NOCc4ccccc4)CC3)sc2C(=O)O)C2CCC(O)CC2)CC1
Reaction #194391
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(S(=O)(=O)C2(Cc3ccccc3)SC(=O)N(CC(=O)NOCc3ccccc3)C2=O)cc1
Reaction #196211
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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