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COC(=O)c1ccnc(N)c1

CCOC(=O)c1cc(-c2ccccc2)[nH]c(=O)c1C(=O)OCC
Reaction #65744
3,4-Diethoxycarbonyl-6-phenyl-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(N(C)C)nc(-c2ccccc2)c(N)c1C(=O)OCC
Reaction #65751
3-Amino-4,5-diethoxycarbonyl-6-dimethylamino-2-phenylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)[nH]c(=O)c1C(=O)OCC
Reaction #65752
3,4-Diethoxycarbonyl-6-methyl-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2ccc(OCOCCOC)cc2)[nH]c(=O)c1C(=O)OCC
Reaction #65765
3,4-Diethoxycarbonyl-6-(4-methoxyethoxymethoxyphenyl)-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(F)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65770
3,4-Diethoxycarbonyl-2-fluoro-5-nitro-6-phenylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-n2cncn2)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65778
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-n2cncn2)nc(-c2ccccc2)c(N)c1C(=O)OCC
Reaction #65779
title compound
Ausbeute 66.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-n2cnnn2)nc(-c2ccccc2)c(N)c1C(=O)OCC
Reaction #65781
title compound
Ausbeute 51.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)c1
Reaction #72040
title compound
Ausbeute 7.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)nc(N2CC[C@H](N)[C@H](OC)C2)c1
Reaction #72041
title compound
Ausbeute 91.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cc(C(=O)OC)cc(C)n3)C[C@H]2OC)nc1Cl
Reaction #72042
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cc(C(=O)OC)cc(Cl)n3)C[C@H]2OC)nc1Cl
Reaction #72069
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(N2CC[C@H](N)[C@H](OC)C2)ncc1C
Reaction #72070
title compound
Ausbeute 18.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)ncc1C
Reaction #72071
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccn2c(C)c(CCc3ccc(C#N)cc3)nc2c1)c1ccccc1
Reaction #78663
3-Methyl-2-[2-(4-cyanophenyl)ethyl]imidazo[1,2-a]pyridin-7-yl-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccn2cc(-c3cc(F)ccc3F)nc2c1
Reaction #88405
title compound
Ausbeute 135.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccnc(/N=C(/c2ccccc2)C(F)(F)F)c1
Reaction #88406
title compound
Ausbeute 27.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccn2c(F)c(-c3ccccc3)nc2c1
Reaction #88407
title compound
Ausbeute 86.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccn(N)c(=[NH2+])c1.Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1
Reaction #88412
title compound
Ausbeute 88.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccn2nc(N)nc2c1
Reaction #88424
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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