Recherche de Sous-structure

271099

COc1cc2c(cc1OC)C(CCc1ccc(C(F)(F)F)cc1)=NCC2
Reaction #188958
DOI: 10.1039/C8SC04228D
CCCC1=NCCc2ccc([N+](=O)[O-])cc21
Reaction #201691
DOI: 10.1039/C8SC04228D
COc1ccc2c(c1)CCN=C2C1CCN(S(=O)(=O)c2cn(C)cn2)CC1
Reaction #225530
DOI: 10.1039/C8SC04228D
CC(C)CNC(=O)c1ccc2c(c1)C(C1CCCCC1)NCC2
Reaction #227149
DOI: 10.1039/C8SC04228D
COc1ccc2c(c1)C(C1CCCCC1)=NCC2
Reaction #231098
DOI: 10.1039/C8SC04228D
COc1ccc2c(c1)CCN=C2C1CCNCC1
Reaction #257255
DOI: 10.1039/C8SC04228D
COc1ccc2c(c1)C(CCc1ccc(F)cc1)NCC2
Reaction #257852
DOI: 10.1039/C8SC04228D
COc1ccc2c(c1)CCNC2C1CCN(S(=O)(=O)c2cn(C)cn2)CC1
Reaction #285760
DOI: 10.1039/C8SC04228D
COC(=O)C1Cc2ccc(O)cc2C(CC2CCCC2)N1
Reaction #286892
DOI: 10.1039/C8SC04228D
NCCOc1ccc2c(c1)C(C1(c3ccc(Cl)cc3)CCC1)=NCC2
Reaction #329223
2-(1-(1-(4-chlorophenyl)cyclobutyl)-3,4-dihydroisoquinolin-7-yloxy)ethanamine
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCOc1ccc2c(c1)C(C1(c3ccc(Cl)cc3)CCC1)=NCC2)c1ccc(Cl)cc1Cl
Reaction #329224
2,4-dichloro-N-(2-{1-[1-(4-chloro-phenyl)-cyclobutyl]-3,4-dihydro-isoquinolin-7-yloxy}-ethyl)-benzamide
Rendement 106.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCOc1ccc2c(c1)C(C1(c3ccc(Cl)cc3)CCC1)NCC2)c1ccc(Cl)cc1Cl
Reaction #329225
2,4-Dichloro-N-(2-{1-[1-(4-chloro-phenyl)-cyclobutyl]-1,2,3,4-tetrahydro-isoquinolin-7-yloxy}-ethyl)-benzamide
Rendement 73.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NCCOc1ccc2c(c1)C(C1(c3ccc(Cl)cc3)CCC1)=NCC2
Reaction #329226
N-(2-{1-[1-(4-Chloro-phenyl)-cyclobutyl]-3,4-dihydro-isoquinolin-7-yloxy}-ethyl)-methanesulfonamide
Rendement 80.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)NCCOc1ccc2c(c1)C(C1(c3ccc(Cl)cc3)CCC1)=NCC2
Reaction #329227
1-(2-{1-[1-(4-Chloro-phenyl)-cyclobutyl]-3,4-dihydro-isoquinolin-7-yloxy}-ethyl)-3-propyl-urea
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)C(C1(c3ccc(Cl)cc3)CCC1)=NCC2
Reaction #329230
final product
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C2(C3=NCCc4ccc(N5CCNCC5)cc43)CCC2)cc1
Reaction #329231
oil
Rendement 69.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)COc2ccc3c(c2)C(C2(c4ccc(Cl)cc4)CCC2)=NCC3)CC1
Reaction #329234
4-(2-{1-[1-(4-Chloro-phenyl)-cyclobutyl]-3,4-dihydro-isoquinolin-7-yloxy}-acetyl)-piperazine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccc2c(c1)C(C1(c3ccc(Cl)cc3)CCC1)=NCC2)N1CCNCC1
Reaction #329235
2-{1-[1-(4-Chloro-phenyl)-cyclobutyl]-3,4-dihydro-isoquinolin-7-yloxy}-1-piperazin-1-yl-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NCCOc1ccc2c(c1)C(C1(c3ccc(Cl)cc3)CCC1)=NCC2)N1CCNCC1
Reaction #329237
desired product
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NCCOc1ccc2c(c1)C(C1(c3ccc(Cl)cc3)CCC1)=NCC2)c1ccc(NCc2ccccc2)nc1
Reaction #329238
solid
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
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