3-bromo-1-methoxybenzene

COc1cccc(N2CCC(C#N)CC2)c1
Reaction #391
Ausbeute 28.5%750 AstraZeneca ELN dataset
COc1cccc(N2CCC(C#N)CC2)c1
Reaction #392
Ausbeute 54.5%750 AstraZeneca ELN dataset
COc1cccc(N2CCC(C(N)=O)CC2)c1
Reaction #393
Ausbeute 0.0%750 AstraZeneca ELN dataset
COc1cccc(N2CCCC2c2cc(C(=O)N(C)C)cc3c(=O)cc(N4CCOCC4)oc23)c1
Reaction #497
Ausbeute 27.5%750 AstraZeneca ELN dataset
COc1cccc(-n2c(C)cc3ccc(OC(F)(F)F)cc32)c1
Reaction #530
Ausbeute 65.5%750 AstraZeneca ELN dataset
COC(=O)c1cc(C2CCCN2c2cccc(OC)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #570
Ausbeute 55.5%750 AstraZeneca ELN dataset
COc1cccc(C(O)(C(F)(F)F)C(F)(F)F)c1
Reaction #4845
1-methoxy-3-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1cccc(-c2ccccn2)c1
Reaction #44321
2-(3-methoxyphenyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cccc(Oc2cccc(O)c2)c1
Reaction #59232
3-(3′-methoxyphenyloxy)phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc[c]([Mg][Br])c1
Reaction #59622
3-methoxyphenylmagnesium bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)c1cc([C@H]2CCCN2c2cccc(OC)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #69476
methyl 8-[(2R)-(1-(3-methoxyphenyl)pyrrolidin-2-yl)]-2-morpholino-4-oxo-4H-chromene-6-carboxylate
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cccc(N2CCN(c3cnccc3C)C2=O)c1
Reaction #167263
product
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cccc(N2CCCCC2)c1
Reaction #176921
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C2(O)CCC3(CC2)OCCO3)c1
Reaction #177755
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)c2cn(-c3cccc(-c4cccnc4F)c3)cn2)c1
Reaction #186275
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)c2ccncc2)c1
Reaction #198086
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(O)c2ccc3c(c2)OCO3)c1
Reaction #203185
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(Br)ccc1S(=O)(=O)Cl
Reaction #217599
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Oc1cccc(-n2cnc(-c3ccccc3)c2)c1
Reaction #225928
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cccc(C(C)C(=O)c2ccccc2)c1
Reaction #231658
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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