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1301906

CC(C)(C)OC(=O)c1ccc(N2CCCCC2)nc1
Reaction #491
Ausbeute 61.9%
COc1cccc(CCc2cc(NC(=O)c3ccc(Cl)nc3)[nH]n2)c1
Reaction #45025
6-chloro-N-[5-[2-(3-methoxyphenyl)ethyl]-2H-pyrazol-3-yl]pyridine-3-carboxamide
Ausbeute 17.3%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2cccc(C(F)(F)F)c2)nc1
Reaction #61788
6-(3-Trifluoromethyl-phenyl)-pyridine-3-carbaldehyde
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Br)nc1
Reaction #65635
methyl 6-bromo-nicotinate
DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc(Br)nc1
Reaction #65636
3-hydroxymethyl-6-bromopyridine
Ausbeute 89.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1ccc(C=O)cn1
Reaction #71634
title compound
Ausbeute 93.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(F)cc1)c1ccc(Br)nc1
Reaction #93812
6-bromo-3-(4-fluorobenzoyl)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(Br)ccc1C(C)=O
Reaction #157733
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(Br)ccc1C=O
Reaction #157734
6-bromo-2-methoxynicotinaldehyde
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(Br)ccc1C=CC(=O)OC(C)(C)C
Reaction #157735
tert-butyl 3-(6-bromo-2-methoxypyridin-3-yl)acrylate
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(C(C)=O)c(OC)n2)c(OC)c1
Reaction #157833
(5R)-5-[(E)-2-(5-acetyl-6-methoxypyridin-2-yl)-2-(4-tert-butylphenyl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCC(c2ccc(-c3ccc(C(=O)Nc4ccc(C(F)(F)F)nc4)cn3)cc2)CC1
Reaction #163267
(4-{4-[5-(6-Trifluoromethyl-pyridin-3-ylcarbamoyl)-pyridin-2-yl]-phenyl}-cyclohexyl)-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(Br)nc1
Reaction #165335
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(C2OCCO2)cn1
Reaction #165336
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(Br)nc1
Reaction #165435
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(C2OCCO2)cn1
Reaction #165436
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2cc3nccc(Oc4ccc([N+](=O)[O-])cc4F)c3s2)nc1
Reaction #171557
title compound 123
Ausbeute 50.2%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2cc3nccc(Cl)c3s2)nc1
Reaction #171561
title compound 136
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCNCc1ccc(Br)nc1
Reaction #171568
143
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(Cc2ccc(N(C)C(=O)c3ccc(N4CCC(F)(F)CC4)nc3)cc2)CCN1C(=O)OC(C)(C)C
Reaction #180048
DOI: 10.1039/C8SC04228D
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