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1274536

CC(C)Oc1cc(I)ccn1
Reaction #68847
4-Iodo-2-isopropoxy-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(I)ccn(-c2ccc(F)cc2)c1=O
Reaction #70998
1-(4-fluorophenyl)-4-iodo-2-oxo-1,2-dihydropyridine-3-carbaldehyde
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c(I)ccn(-c2ccc(F)cc2)c1=O
Reaction #70999
desired product
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1nccc(Oc2ccc(NC(=O)c3c(I)ccn(-c4ccc(F)cc4)c3=O)cc2F)c1Cl
Reaction #71000
desired product
Ausbeute 88.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccn(-c2ccc(F)cc2)c(=O)c1C(=O)Nc1ccc(Oc2ccnc(C(N)=O)c2Cl)c(F)c1
Reaction #71001
desired product
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)OCC)n1ccc(I)cc1=O
Reaction #84935
Ethyl 2-(4-iodo-2-oxopyridin-1(2H)-yl)hexanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)OCC)n1ccc(-c2cc(Cl)ccc2C#N)cc1=O
Reaction #84936
Ethyl 2-[4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]hexanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cn(C(C)C(=O)Nc2ccc(C(=O)OC(C)(C)C)cc2)c(=O)cc1-c1cc(Cl)ccc1C#N
Reaction #85032
tert-Butyl 4-({2-[4-(5-chloro-2-cyanophenyl)-5-isopropoxy-2-oxopyridin-1(2H)-yl]propanoyl}amino)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCn1ccc(I)cc1=O
Reaction #163305
4-Iodo-N-propyl-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(I)ccn1
Reaction #163310
4-Iodo-2-isopropoxy-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(-n3cccn3)cc2)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171397
residue
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(/C=C/c2ccccc2)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171399
residue
Ausbeute 47.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(OC[C@H]3CC[C@H](OC4CCCCO4)CC3)cc2)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171415
title compound
Ausbeute 49.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(OC[C@H]3CC[C@H](OC4CCCCO4)CC3)cc2F)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171418
title compound
Ausbeute 795.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2cc(-c3ccn(CC[C@](C)(C(=O)NO)S(C)(=O)=O)c(=O)c3)ccc2[nH]1
Reaction #171426
light brown solid
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(CCn1ccc(-c2ccc(OCCCO)cc2)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171432
4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(CCn1ccc(-c2ccc(-c3ccncc3)cc2)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171441
title product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(F)cc2)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171444
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(Cl)c(F)c2F)cc1=O)(C(=O)O)S(C)(=O)=O
Reaction #171449
title compound
Ausbeute 89.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(I)cc[nH]c1=O
Reaction #171456
4-iodo-3-methylpyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
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