An 29 Reaktionen beteiligt

23921

Clc1cc(-c2cncc(Br)c2)ccn1
Reaction #171357
5-bromo-2′-chloro-[3,4′]bipyridinyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[Si](C)(C)C#Cc1cncc(Br)c1
Reaction #197682
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCN(c2cncc(Br)c2)CC1
Reaction #262655
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Brc1cncc(-c2cnn(CCN3CCCC3)c2)c1
Reaction #288606
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CCN(c2cncc(Br)c2)CC1
Reaction #357731
desired product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Brc1cncc(-c2cc3ccccc3[nH]2)c1
Reaction #680771
2-(5-bromopyridin-3-yl)-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
C[Si](C)(C)C#Cc1cncc(Br)c1
Reaction #693985
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CSc1cncc(Br)c1
Reaction #693992
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CSc1cncc(Br)c1
Reaction #763071
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C1OCCN1c1cncc(Br)c1
Reaction #799943
3-(5-bromo-pyridin-3-yl)-oxazolidin-2-one
Ausbeute 232.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CC(C)(C)OC(=O)N1CCC(n2cc(-c3cncc(Br)c3)cn2)CC1
Reaction #918368
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(c2cncc(Br)c2)CC1
Reaction #1131744
desired product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
Cn1cc(-c2cncc(Br)c2)cn1
Reaction #1296240
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CC(C)(C)OC(=O)N1CCN(c2cncc(Br)c2)CC1
Reaction #1348825
desired product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
Cn1cc(-c2cncc(Br)c2)cn1
Reaction #1491471
3-bromo-5-(1-methyl-1H-pyrazol-4-yl)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CC(C)(C)OC(=O)N1CCC(n2cc(-c3cncc(Br)c3)cn2)CC1
Reaction #1491473
4-[4-(5-bromo-pyridin-3-yl)-pyrazol-1-yl]-piperidine-1-carboxylic acid tert-butyl-ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Brc1cncc(-c2cnn(CCN3CCCC3)c2)c1
Reaction #1491477
3-bromo-5-[1-(2-pyrrolidin-1-yl-ethyl)-1H-pyrazol-4-yl]-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CC(C)(C)OC(=O)N1CCN(c2cncc(Br)c2)CC1
Reaction #1523944
desired product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11
CC(C)(C)OC(=O)NC1CCN(c2cncc(Br)c2)CC1
Reaction #1616512
tert-butyl 1-(5-bromopyridin-3-yl)piperidin-4-ylcarbamate
Ausbeute 26.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
CC(C)(C)OC(=O)N1CCCC(Nc2cncc(Br)c2)C1
Reaction #1616520
tert-butyl 3-(5-bromopyridin-3-ylamino)piperidine-1-carboxylate
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
Seite 1Weiter