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1147607

O=C1COCCN1c1cccc(Br)n1
Reaction #768
Ausbeute 68.8%
Brc1cccc(NC2CCOCC2)n1
Reaction #823
Ausbeute 0.0%
Fc1ccc(C23CCCN2CCC3)c(F)n1
Reaction #3389
oil
Ausbeute 50.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cccc(F)n2)c(OC)n1
Reaction #40981
title compound
Ausbeute 57.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)c1ccc(F)nc1F
Reaction #44617
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(=O)c1cccc(Br)n1
Reaction #45389
6-Bromo-pyridine-2-carboxylic acid tert-butylamide
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cccc(Sc2ccccc2)n1
Reaction #55981
2-bromo-6-phenylthiopyridine
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(Br)=N/C(=C\C)C(=O)CCC(OC)OC
Reaction #57360
N-[1-Eth-(Z)-ylidene-5,5-dimethoxy-2-oxo-pentyl]-acrylimidoyl bromide
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)Nc1c(-c2ccc(C#Cc3cccc(F)n3)s2)nc2cnccn12
Reaction #57391
N-tert-butyl-2-(5-((6-fluoropyridin-2-yl)ethynyl)thiophen-2-yl)imidazo[1,2-a]pyrazin-3-amine
Ausbeute 30.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)c2cccc(Br)n2)CC1
Reaction #58493
2-bromo-6-(1-t-butoxycarbonylpiperidin-4-ylcarbonyl)-pyridine
Ausbeute 100.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(C(=O)c2cccc(Br)n2)CC1
Reaction #58496
2-bromo-6-(1-methylpiperidin-4-ylcarbonyl)-pyridine
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(C(=O)c2cccc(Br)n2)CC1
Reaction #58505
title intermediate
Ausbeute 85.3%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(Br)n1
Reaction #58751
title compound
Ausbeute 52.1%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(Br)n1
Reaction #60012
2-bromo-6-formylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
FC1(F)CC1COc1cccc(Br)n1
Reaction #68789
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(Br)n1
Reaction #71059
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(c2ccc(-c3ccc(-c4onc(C)c4Nc4cccc(Br)n4)cc3)cc2)CC1
Reaction #73880
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(n1)OC1(C2)CN2CCC1CC2
Reaction #76807
sub-title compound
Ausbeute 8.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(F)nc1F
Reaction #79111
2,6-difluoronicotinic acid
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1cccc(-n2c(/C=C/c3ccccc3)nc3ccccc32)n1
Reaction #79152
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
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