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27448

O=C(O)c1cc(Br)cnc1Cl
Reaction #4890
5-Bromo-2-chloro-3-pyridinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)cnc1O
Reaction #4891
product
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)cnc1N
Reaction #46532
title compound
Ausbeute 98.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNC(=O)Nc1ncc(Br)cc1C(=O)O
Reaction #88718
5-bromo-2-(3-(3-methoxy-3-oxopropyl)ureido)nicotinic acid
Ausbeute 58.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccc(C(=O)NNC(=O)c2nc(Br)cnc2N)cc1)C(=O)OC(C)(C)C
Reaction #165848
product
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2ccc(Cl)cc2)cn1
Reaction #202252
DOI: 10.1039/C8SC04228D
O=C(O)c1cc(Br)cnc1O
Reaction #234079
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(F)cc1F)c1cc(Br)cnc1F
Reaction #273795
DOI: 10.1039/C8SC04228D
Nc1ncc(Br)cc1C(=O)c1ccccc1
Reaction #286316
DOI: 10.1039/C8SC04228D
Nc1ncc(Br)cc1C(=O)NCCO
Reaction #313041
compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)cnc1Cl
Reaction #323318
5-Bromo-2-chloro-3-pyridinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)cnc1O
Reaction #323319
product
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)cnc1O
Reaction #325666
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Cl)cc1)c1cc(Br)cnc1Cl
Reaction #325667
5-bromo-2-chloro-N-(4-chlorophenyl)nicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1cc(Br)cnc1N
Reaction #328241
title Compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(Br)cc1-c1nc2ncccc2[nH]1
Reaction #328594
5-bromo-3-(1H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)cnc1Cl
Reaction #334444
5-Bromo-2-chloro-3-pyridinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)cnc1O
Reaction #334445
product
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc(Br)cnc1Cl
Reaction #341137
5-bromo-2-chloropyridine-3-carbonyl chloride
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)c1cc(Br)cnc1Cl
Reaction #374779
DOI: 10.1039/C8SC04228D
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