ethyl 2-oxoacetate

CCOC(=O)CNc1cc(Cl)cnc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11816
title compound
Ausbeute 66.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C1CC(=O)C=CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44018
compound 103
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCc1nc2c(n1Cc1ccc(-c3ccccc3-c3nnn[nH]3)cc1)C(C(=O)OCC)NCC2
Reaction #50138
ethyl 2-n-butyl-3-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate
Ausbeute 44.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CO.ClCCl.[NH4+].[OH-]
Reaction #51481
CH2Cl2 MeOH ammonium hydroxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)C1Nc2ccc(OC(F)(F)F)cc2C2CCCCCCC12
Reaction #75698
Compound 76
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)C1CC(c2cc3c(cc2Cl)OCO3)c2cc(C(C)CC)ccc2N1
Reaction #75699
Compound 77
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)C(O)CC1CC1
Reaction #84938
Ethyl 3-cyclopropyl-2-hydroxypropanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)C(O)CC1CCC1
Reaction #85096
Ethyl 3-cyclobutyl-2-hydroxypropanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1cnco1
Reaction #86940
ethyl oxazole-5-carboxylate
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)C(O)NC(=O)OCc1ccccc1
Reaction #93458
ethyl 2-(benzyloxycarbonylamino)-2-(hydroxy)acetate
Ausbeute 64.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCOC(=O)c1cncn1-c1ccc(CC)cc1
Reaction #159896
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)CNc1ccc(-c2cc(Cc3ccc(OCc4ccccc4)nc3)no2)c(N)n1
Reaction #165458
title compound
Ausbeute 8.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(=O)Nc1ncc(Br)nc1NCc1c(F)ccc(F)c1Cl
Reaction #167718
ethyl ({5-bromo-3-[(2-chloro-3,6-difluorobenzyl)amino]pyrazin-2-yl}amino)(oxo)acetate
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C=NC(C)(C)CO
Reaction #175093
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C=C1SC(c2ccccc2)N(CCC(C)C)C1=O
Reaction #177765
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(O)C(C)C(=O)c1cnc(-c2ccccc2)s1
Reaction #177878
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CNCCCCC(NC(CCc1ccccc1)C(=O)O)C(=O)N1CCCC1C(=O)O
Reaction #180914
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1C(OCc2ccccc2)C(=O)N1c1ccc(OC)cc1
Reaction #181394
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CN(C(=O)OCC)C(CC)Cc1cccs1
Reaction #185892
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1OC(O)CS1
Reaction #186299
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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