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O=C(Cl)c1ccccn1

CC(=O)Oc1cnc(C(=O)Cl)cc1OC(C)=O.Cl
Reaction #5616
4,5-diacetoxy-2-pyridinecarbonyl chloride hydrochloride
Ausbeute 158.5%DOI: 10.6084/m9.figshare.5104873.v1
CCON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])=C(C[N+]3(C)CCN(C(=O)c4cc(O)c(O)cn4)CC3)CS[C@H]12)c1nsc(N)n1
Reaction #5627
7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-ethoxyiminoacetamido]-3-[1-methyl-4-(4,5-dihydroxy-2-pyridylcarbonyl)-1-piperazinio]methyl-3-cephem-4-carboxylate
Ausbeute 47.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccccn4)c3C2=O)C(=O)N1
Reaction #10082
product
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1cc(Cl)ccn1
Reaction #41799
desired product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #56981
solid
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #56985
solid
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccccn1
Reaction #63227
picolinic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCO)c1ccccn1
Reaction #63228
N-(2-Hydroxyethyl)pyridine-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(NCc1ccncc1)c1cccc(C(=O)N2Cc3ccccc3Oc3ccc(Cl)cc32)n1
Reaction #65634
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Oc2cccc(Cl)c2)c(Cl)c1)c1ccccn1
Reaction #66521
N-(3-chloro-4-(3-chlorophenoxy)phenyl)picolinamide
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(=O)c2ccccn2)ccc1Oc1ncccn1
Reaction #66524
N-(3-methoxy-4-(pyrimidin-2-yloxy)phenyl)picolinamide
Ausbeute 19.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)N1CCN(c2ccc(NC(=O)c3ccccn3)cc2Cl)CC1
Reaction #66527
N-(3-chloro-4-(4-isobutyrylpiperazin-1-yl)phenyl)picolinamide
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(NC(=O)c3ccccn3)cc2Cl)CC1
Reaction #66529
tert-butyl 4-(2-chloro-4-(picolinamido)phenyl)piperazine-1-carboxylate
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(=O)N(c2cc(C#CC(C)(C)C)sc2C(=O)O)C2CCN(C(=O)c3cccnc3)CC2)CC1
Reaction #67592
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(=O)N(c2cc(C#CC(C)(C)C)sc2C(=O)O)C2CCN(C(=O)c3cccnc3)C2)CC1
Reaction #67593
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CNCCN1C(=O)c1ccccn1.Cl.Cl
Reaction #69581
title compound
Ausbeute 100.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(C(=O)c2ccccn2)CCN1S(=O)(=O)c1ccc(Cl)cc1.Cl
Reaction #69588
title compound
Ausbeute 72.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(S(=O)(=O)c2ccc(Cl)cc2)CCN1C(=O)c1ccccn1
Reaction #69593
title compound
Ausbeute 45.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cccc(-c2ccccc2)n1
Reaction #74196
6-Phenyl-pyridine-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H](CC(=O)c1cccc(-c2ccccc2)n1)C(=O)O
Reaction #74197
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
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