N-methoxymethanamine

CON(C)C(=O)c1ccc2ncccc2c1
Reaction #44300
quinoline-6-carboxylic acid methoxy-methyl-amide
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CON(C)C(=O)C1CCC(NC(=O)OC(C)(C)C)CC1
Reaction #58036
[4-(methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CON(C)C(=O)[C@H](C)[C@H]1COC(=O)N1
Reaction #85654
(R)—N-methoxy-N-methyl-2-((S)-2-oxooxazolidin-4-yl)propanamide
Ausbeute 195.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CON(C)C(=O)Nc1ccc(OCCc2ccc(C)cc2)cc1
Reaction #94097
N'-[4-(4-methylphenethyloxy)phenyl]-N-methoxy-N-methylurea
Ausbeute 108.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CON(C)C(=O)Nc1ccc(OCCc2ccc(C(C)C)cc2)cc1
Reaction #94098
N'-[4-(4-isopropylphenethyloxy)phenyl]-N-methoxy-N-methylurea
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CON(C)C(=O)c1ccc2c(c1)OCCc1cc(C(=O)N(C)c3ccccc3Cl)sc1-2
Reaction #171679
188
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CON(C)C(=O)C(C)NC(=O)OC(C)(C)C
Reaction #173024
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON(C)C(=O)C1CCN(C(c2ccccc2)(c2ccccc2)c2ccccc2)CC1
Reaction #174332
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON(C)C(=O)c1ccc(F)c(O)c1
Reaction #174470
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1ccc(-c2nc(CCC(=O)N(C)OC)cs2)cc1OCC
Reaction #175667
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON(C)C(=O)c1ccc2c(c1)OCO2
Reaction #175823
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON(C)C(=O)C1CCCN1C(=O)OC(C)(C)C
Reaction #176889
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON(C)C(=O)CC1CC(CO)OC(C)(C)O1
Reaction #177625
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON(C)C(=O)C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #178982
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(Cn2cc(C(=O)N(C)OC)c(=O)c3ccccc32)cc1
Reaction #179469
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON(C)C(=O)C1CCCN(C(=O)OC(C)(C)C)C1
Reaction #179527
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON(C)C(=O)CCc1ccccc1
Reaction #179626
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(C(=O)N(C)OC)c1ccc(-c2nnn(C)n2)cc1
Reaction #182378
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON(C)C(=O)c1nc(C)cc2c1c(=O)cc(Nc1ccccc1)n2-c1ccccc1
Reaction #182929
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON(C)C(=O)CCCCO
Reaction #184398
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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