Ähnlichkeitssuche

18598

COc1ccc2c(c1)c1c3c(c(-c4ccccc4Cl)cc1n2CCCO)C(=O)NC3=O
Reaction #11134
4-(2-Chlorophenyl)-6-(3-hydroxypropyl)-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c3c(c(-c4ccccc4Cl)cc1n2CCO)C(=O)NC3=O
Reaction #11137
4-(2-Chlorophenyl)-6-(2-hydroxyethyl)-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c1c(-c1ccccc1Cl)cc1c2c2cc(O)ccc2n1CCO
Reaction #11138
4-(2-Chlorophenyl)-6-(2-hydroxyethyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c1c(-c1ccccc1Cl)cc1c2c2cc(O)ccc2n1CCCO
Reaction #11156
4-(2-Chlorophenyl)-9-hydroxy-6-(3-hydroxypropyl)pyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c3c(c(-c4ccccc4Cl)cc1n2CCC#N)C(=O)NC3=O
Reaction #11160
nitrile
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1
N#CCCn1c2ccc(O)cc2c2c3c(c(-c4ccccc4Cl)cc21)C(=O)NC3=O
Reaction #11161
phenol
Ausbeute 89.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c3c(c(-c4c(Cl)cccc4Cl)cc1n2CCC(N)=O)C(=O)NC3=O
Reaction #11199
amide
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCNC(=O)CCn1c2ccc(O)cc2c2c3c(c(-c4ccccc4)cc21)C(=O)NC3=O
Reaction #11200
N-[2-(Dimethylamino)ethyl]-3-(9-hydroxy-1,3-dioxo-4-phenyl-2,3-dihydropyrrolo[3,4-c]carbazol-6 (1H)-yl)propanamide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CCn1c2ccc(O)cc2c2c3c(c(-c4c(Cl)cccc4Cl)cc21)C(=O)NC3=O
Reaction #11201
amide
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(Cl)c1-c1cc2c(c3c1C(=O)NC3=O)c1cc(O)ccc1n2CCC(=O)NCCN(C)C
Reaction #11202
amide
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1cc2c(c3c1C(=O)NC3=O)c1cc(O)ccc1n2CCC(=O)NCCN(C)C
Reaction #11203
amide
Ausbeute 17.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCS(=O)(=O)NC(=O)CCn1c2ccc(O)cc2c2c3c(c(-c4ccccc4Cl)cc21)C(=O)NC3=O
Reaction #11204
acylsulfonamide
Ausbeute 23.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCn1c2ccc(O)cc2c2c3c(c(-c4ccccc4Cl)cc21)C(=O)NC3=O
Reaction #11205
( 117 )
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CCn1c2ccc(O)cc2c2c3c(c(-c4ccccc4Cl)cc21)C(=O)NC3=O
Reaction #11206
( 119 )
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c3c(c(-c4ccccc4Cl)cc1n2CCC(=O)NCCN1CCOCC1)C(=O)NC3=O
Reaction #11207
amide
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCn1c2ccc(O)cc2c2c3c(c(-c4ccccc4Cl)cc21)C(=O)NC3=O)NCCN1CCOCC1
Reaction #11208
( 121 )
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c3c(c(-c4ccccc4Cl)cc1n2CCC(=O)NC1CC(C)(C)NC(C)(C)C1)C(=O)NC3=O
Reaction #11209
amide
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(NC(=O)CCn2c3ccc(O)cc3c3c4c(c(-c5ccccc5Cl)cc32)C(=O)NC4=O)CC(C)(C)N1
Reaction #11210
( 125 )
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c3c(c(-c4ccccc4Cl)cc1n2CCC(=O)N1C[C@@H](C)N[C@@H](C)C1)C(=O)NC3=O
Reaction #11211
amide
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)CCn2c3ccc(O)cc3c3c4c(c(-c5ccccc5Cl)cc32)C(=O)NC4=O)C[C@H](C)N1
Reaction #11212
( 127 )
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
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