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757881

Cc1c(N2CC3C(OC(=O)c4ccccc4)CCC3C2=O)ccc(C#N)c1Cl
Reaction #43466
title compounds 1K
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(Cl)cc1I
Reaction #44359
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccccc1)N1C(=O)c2c(I)cc(Cl)c(Cl)c2C1O
Reaction #49514
3-hydroxy-4,5-dichloro-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCc2c(Cl)c(Cl)cc(I)c21
Reaction #49515
4,5-dichloro-7-iodoisoindolinone
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccncc1Nc1ccc(I)cc1Cl
Reaction #67784
3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccncc1Nc1ccc(I)cc1Cl
Reaction #67796
3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NOC[C@H](O)CO)c1ccncc1Nc1ccc(I)cc1Cl
Reaction #67797
3-[(2-chloro-4-iodophenyl)amino]-N-{[(2R)-2,3-dihydroxypropyl]oxy}isonicotinamide
Ausbeute 43.6%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccncc1Nc1ccc(I)cc1Cl
Reaction #67798
3-[(2-chloro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccncc1Nc1ccc(I)cc1Cl
Reaction #67807
3-[(2-chloro-4-iodophenyl)amino]-N-methylisonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(Nc2cnccc2C(=O)NOCC(O)CO)c(Cl)c1
Reaction #67835
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=CCONC(=O)c1ccncc1Nc1ccc(I)cc1Cl
Reaction #67852
N-allyloxy-3-(2-chloro-4-iodo-phenylamino)-isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NOCc1ccccc1)c1ccncc1Nc1ccc(I)cc1Cl
Reaction #67855
N-Benzyloxy-3-(2-chloro-4-iodo-phenylamino)-isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(S(=O)(=O)Nc2ncc(Cl)s2)ccc1Oc1ccc(Cl)cc1-c1cn[nH]c1
Reaction #74515
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(S(=O)(=O)Nc2ncns2)ccc1Oc1ccc(Cl)cc1-c1cn[nH]c1
Reaction #74519
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(S(=O)(=O)Nc2ncc(Cl)s2)ccc1Oc1ccc(Cl)cc1I
Reaction #74581
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(c1cscn1)S(=O)(=O)c1ccc(Oc2ccc(Cl)cc2I)c(C#N)c1
Reaction #74598
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Cl)c([N+](=O)[O-])c(I)c2[nH]c1=O
Reaction #82038
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Cl)cc(I)c2[nH]c1=O
Reaction #82624
5-iodo-7-chloro-1,4-dihydro-2,3-quinoxalinedione
Ausbeute 74.2%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Cl)c([N+](=O)[O-])c(I)c2[nH]c1=O
Reaction #82625
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)(CSCC(F)(F)F)c1cc2cc(Cl)c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #84231
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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