pyridin-2-ylmethanol

COc1cccc(Oc2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCc2ccccn2)c1
Reaction #2362
4-tert-butyl-N-{5-(3-methoxyphenoxy)-6-(2-pyridinylmethoxy)pyrimidin-4-yl}benzenesulfonamide
Ausbeute 94.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)Cc1ccc(C(C)C(=O)OCc2ccccn2)cc1
Reaction #54733
2-(4-isobutylphenyl)propionic acid-2-pyridylmethyl ester
Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=[N+]([O-])c1ccc(OCc2ccccn2)c(Cl)c1
Reaction #66786
title compound
Ausbeute 48.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(-c2cn(C3CCOCC3)c3ncnc(N)c23)ccc1NC(=O)OCc1ccccn1
Reaction #79748
2-pyridylmethyl N-[4-(4-amino-7-tetrahydro-2H-4-pyranyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-2-methoxyphenyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cc(-c2cn(C3CCOCC3)c3ncnc(N)c23)ccc1NC(=O)OCc1ccccn1
Reaction #79829
2-pyridylmethyl N-[4-(4-amino-7-tetrahydro-2H-4-pyranyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-2-methoxyphenyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)[C@@H](NC(=O)OCc1ccccn1)C(C)C
Reaction #82194
desired compound
Ausbeute 54.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(NC1CCC(COC(=O)N2CCCC2)CC1)OCc1ccccn1
Reaction #155670
compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=Cc1ccc(OCc2ccccn2)c(F)c1
Reaction #165236
title compound
Ausbeute 45.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=S(=O)(Nc1nccnc1OCc1ccccn1)c1cccc(Cl)c1Cl
Reaction #182946
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccccc1-c1nc(N)nc(OCc2ccccn2)c1C#N
Reaction #184340
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cnc(NS(=O)(=O)c2cccc(Cl)c2Cl)c(OCc2ccccn2)n1
Reaction #185716
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ncc(OCc2ccccn2)nc1NCc1ccc(OC)c(Cl)c1
Reaction #200294
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(C(=O)NC2CC2)cc1NC(=O)c1cc(F)c(OCc2ccccn2)c(F)c1
Reaction #231581
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(COc2nn3c(-c4cccs4)nnc3cc2C2CCCC2)nc1
Reaction #239684
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(OCC)c1c(F)cc(OCc2ccccn2)cc1F
Reaction #240937
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=S(=O)(c1ccc(Cl)cc1)C(Cc1ccccn1)c1cc(F)ccc1F
Reaction #250299
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCc1ccccn1
Reaction #251607
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1ccc(OCc2ccccn2)c(Cl)c1
Reaction #260436
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1nc(OCc2ccccn2)c(Br)c(-c2ccco2)n1
Reaction #262154
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CS(=O)(=O)OCc1ccccn1
Reaction #265263
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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