O-methylhydroxylamine;hydrochloride

CON=Cc1[nH]ccc1S(=O)(=O)NC(C)(C)C
Reaction #917
title compound
收率 96.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CON=C(C)c1cccc(Sc2nc(OC)cc(OC)n2)c1C(=O)OC
Reaction #4999
aimed compound
收率 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CON=C(C)c1cccc(ON2N=C(OC)C=C(OC)N2)c1C(=O)OC
Reaction #5004
aimed compound
收率 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CON=C1C[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H]1CO[Si](C)(C)C(C)(C)C
Reaction #6047
title compound
收率 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CON=C1CC(CO[Si](C)(C)C(C)(C)C)(CO[Si](C)(C)C(C)(C)C)C1
Reaction #6061
title compound
收率 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cccc([N+](=O)[O-])c1N
Reaction #7184
2-amino-3-methoxy-nitrobenzene
收率 50.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Nc1cccc(-c2ccccc2)c1[N+](=O)[O-]
Reaction #7186
2-amino-6-phenyl-nitrobenzene
收率 27.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #40624
solid
收率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #40643
solid
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CON=C(C)c1ccc(-c2ccc(C(F)(F)F)cc2)c(-c2ccccc2)n1
Reaction #40840
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(=NOC)c1ccc(-c2ccc(C(F)(F)F)cc2)c(-c2ccccc2)n1
Reaction #40841
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41806
2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CONC(=O)Nc1ccc(-c2sc3c(c2CN(C)Cc2ccccc2)c(=O)n(-c2ccccc2)c(=O)n3Cc2c(F)cccc2F)cc1
Reaction #51533
5-(N-benzyl-N-methylaminomethyl)-1-(2,6-difluorobenzyl)-6-[4-(3-methoxyureido)phenyl]-3-phenylthieno[2,3-d]pyrimidine-2,4(1H, 3H)-dione
收率 98.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CONC(=O)Nc1ccc(-c2sc3c(c2CN(C)Cc2ccccc2)c(=O)n(-c2ccccc2)c(=O)n3Cc2c(F)cccc2F)cc1
Reaction #51534
5-(N-benzyl-N-methylaminomethyl)-1-(2,6-difluorobenzyl)-6-[4-(3-methoxyureido)phenyl]-3-phenylthieno[2,3-d]pyrimidine-2,4(1H, 3H)-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CONC(=O)Nc1ccc(-c2sc3c(c2CN(C)Cc2ccccc2)c(=O)n(-c2ccccc2)c(=O)n3Cc2c(F)cccc2F)cc1
Reaction #51535
5-(N-benzyl-N-methylaminomethyl)-l-(2,6-difluorobenzyl)-6-[4-(3-methoxyureido)phenyl]-3-phenylthieno[2,3-d]pyrimidine-2,4(1H, 3H)-dione
收率 92.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #54986
Formula II
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CON=C(C(=O)NC1C(=O)N2C(C(=O)O)=CC(C)S[C@H]12)c1csc(NC=O)n1
Reaction #56571
2-methyl-7-[2-methoxyimino-2-(2-formylaminothiazol-4-yl)acetamido]-3-cephem-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
OC[C@H]1O[C@@H](N2c3cc(Cl)c(Cl)cc3C(=C=NO)C2Cl)[C@H](O)[C@@H]1O
Reaction #56628
4.29
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CON=C=C1c2cc(Cl)c(Cl)cc2N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C1Cl
Reaction #56629
4.30
收率 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CON=C(C)c1ccc(-c2ccc(C=CC(=N)Nc3ccc(Cl)cc3)cc2)cc1
Reaction #58717
N-(4-chloro-phenyl)-3-[4′-(1-methoxyimino-ethyl)-biphenyl-4-yl]-acrylamidine
收率 9.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
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