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763065

Nc1ncc2cc(-c3c(Cl)cccc3Cl)c(=O)n(Cc3ccncc3)c2n1
Reaction #3328
2-amino-6-(2,6-dichlorophenyl)-8-pyridin-4-ylmethyl-8H-pyrido[2,3-d]pyrimidin-7-one
DOI: 10.6084/m9.figshare.5104873.v1
Cl.ClCc1ccncc1
Reaction #8506
( 21 )
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1ccncc1)C(C)=O
Reaction #11547
ethyl 2-acetyl-3-(4-pyridyl)propionate
Ausbeute 19.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc2nc(-c3c(Cl)cccc3Cl)ccc2c1)NC(=O)c1c(Cl)cncc1Cl
Reaction #43698
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(N5CCN(Cc6ccncc6)C5=O)c4)CC3)cccc2n1.Cl.Cl
Reaction #44166
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1ccncc1)C(C)=O
Reaction #46671
ethyl 2-acetyl-3-(4-pyridyl)propionate
Ausbeute 19.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2CCc3cccc(NC(=O)c4ccncc4)c32)cc1
Reaction #46977
compound 26
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OCc1ccncc1
Reaction #49651
4-(Isopropoxymethyl)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N(NC(=O)c1ccccc1)C(=O)c1ccncc1
Reaction #49921
N'-t-butyl-N-benzoyl-N'-isonicotinoylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N(NCc1ccncc1)C(=O)c1ccccc1
Reaction #49932
N'-t-butyl-N-isonicotinyl-N'-benzoylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(N2CCOCC2)c2ccccc2C1(Cc1ccncc1)Cc1ccncc1
Reaction #50510
desired product
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(N2CCOCC2)c2ccccc2C1(Cc1ccnc(F)c1)Cc1ccnc(F)c1
Reaction #50511
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Sc1ccccn1)c1ccncc1
Reaction #51584
crystals
Ausbeute 77.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1c(Cl)cncc1Cl
Reaction #52166
3,5-Dichloropyridine-4-carboxylic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1c(Cl)cncc1Cl
Reaction #52167
3,5-dichloropyridine-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC/C(C)=C/CC/C(=C\CC/C(C)=C/CO)CO.O=C(O)c1ccncc1.O=C(O)c1ccncc1
Reaction #55266
end product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)c1ccncc1
Reaction #59667
N-Phenylisonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(Cl)c1ccncc1
Reaction #70906
Isonicotinoyl Chloride Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1n[nH]c2nc(-c3ccc(F)cc3)c(-c3ccncc3)cc12)c1ccncc1
Reaction #70907
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc2c3c(c1)CCN3C(=O)CC2
Reaction #72473
product
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1
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