2-chloro-5-chloromethyl pyridine

Clc1ccc(COc2ccc(Oc3ccccc3)cc2Cl)cn1
Reaction #5300
2-chloro-5-(2-chloro-4-phenoxyphenoxy)methylpyridine
Ausbeute 70.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
FC(F)(F)c1cccc(Oc2ccc(OCc3ccc(Cl)nc3)c(Cl)c2)c1
Reaction #5301
2-chloro-5-[2-chloro-4-(3-trifluoromethylphenoxy)phenoxy]methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Clc1ccc(COc2ccc(Oc3cccc(Br)c3)cc2Cl)cn1
Reaction #5302
2-chloro-5-[4-(3-bromophenoxy)-2-chlorophenoxy]methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=[N+]([O-])C=C1SCCN1Cc1ccc(Cl)nc1
Reaction #50485
3-(2-chloro-5-pyridylmethyl)-2-nitromethylenethiazolidine
Ausbeute 29.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=[N+]([O-])N=C1SCCN1Cc1ccc(Cl)nc1
Reaction #50494
3-(2-chloro-5-pyridylmethyl)-2-(nitroimino)thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=c1ccc2cc(OCc3ccc(Cl)nc3)ccc2[nH]1
Reaction #164623
6-((6-chloropyridin-3-yl)methoxy)quinolin-2(1H)-one
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N1CCN(Cc2ccc(Cl)nc2)CC1
Reaction #166383
compound 339
Ausbeute 84.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)CN1CCN(Cc2ccc(Cl)nc2)CC1
Reaction #166388
compound 348
Ausbeute 30.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1CN(Cc2ccc(Cl)nc2)CCN1
Reaction #166393
compound 356
Ausbeute 34.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N1CCN(Cc2ccc(Cl)nc2)C(=O)C1
Reaction #166395
compound 358
Ausbeute 93.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CSCc1ccc(Cl)nc1
Reaction #178430
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(Cc1ccc(Cl)nc1)C(C)(C)C
Reaction #179279
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc(C#Cc2ccnc(Cl)c2)cn1Cc1ccc(Cl)nc1
Reaction #179915
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)CNCc1ccc(Cl)nc1
Reaction #192867
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
ClC(Cl)=CCOc1cc(Cl)c(OCc2ccc(Cl)nc2)c(Cl)c1
Reaction #194913
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)Cc1c(C(=O)OCC)c2cc(Oc3ccc(CCl)cn3)ccc2n1-c1ccc(OC(C)C)cc1
Reaction #202985
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ccc(CN2CCCCCC2)cn1
Reaction #203526
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(Cc1ccc(Cl)nc1)C1CCCCC1
Reaction #204257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)Cc1c(C(=O)OCC)c2cc(Oc3ccc(CCl)cn3)ccc2n1-c1ccc(OC(F)(F)F)cc1
Reaction #206306
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(C)(Cc1ccc(Cl)nc1)C(=O)OC
Reaction #231852
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Seite 1Weiter