Teilstruktursuche

1300218

CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(CNCc3ccc4c(c3)CCC(=O)N4Cc3ccccc3)ccc21
Reaction #156158
title compound
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc2c(c1)CCCN2Cc1ccccc1
Reaction #206169
DOI: 10.1039/C8SC04228D
O=Cc1cc2c(cc1O)N(Cc1ccccc1)CCC2
Reaction #218357
title compound
Ausbeute 15.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(cc1O)N(Cc1ccccc1)CCC2
Reaction #218358
title compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(c1ccc2c(c1)CCC(=O)N2Cc1ccccc1)N1CCN(CCOc2ccccc2)CC1
Reaction #445688
1-benzyl-6-[4-(2-phenoxyethyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc2c(c1)CCCN2Cc1ccccc1)N1CC(N2CCN(C(=O)c3nccs3)CC2)C1
Reaction #488830
compound 370
Ausbeute 764.6%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc2c(c1)CCCN2Cc1ccccc1
Reaction #533220
Compound 6
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc2c(c1)CCCN2Cc1ccccc1)N1CC(N2CCN(C(=O)c3nccs3)CC2)C1
Reaction #555302
compound 370
Ausbeute 764.6%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc2c(c1)CCCN2Cc1ccccc1
Reaction #736376
1-Benzyl-1,2,3,4-tetrahydro-6-quinolinecarbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc2c(cc1O)N(Cc1ccccc1)CCC2
Reaction #944141
title compound
Ausbeute 15.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(cc1O)N(Cc1ccccc1)CCC2
Reaction #944142
title compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc2c(c1)CCCN2Cc1ccccc1)N1CC(N2CCN(C(=O)c3nccs3)CC2)C1
Reaction #1110251
compound 370
Ausbeute 764.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(c1ccc2c(c1)CCC(=O)N2Cc1ccccc1)N1CCN(CCOc2ccccc2)CC1
Reaction #1241177
1-benzyl-6-[4-(2-phenoxyethyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc2c(c1)CCCN2Cc1ccccc1
Reaction #1300242
DOI: 10.1039/C8SC04228D
Cl.O=C(c1ccc2c(c1)CCC(=O)N2Cc1ccccc1)N1CCN(CCOc2ccccc2)CC1
Reaction #1350040
1-benzyl-6-[4-(2-phenoxyethyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(CNCc3ccc4c(c3)CCC(=O)N4Cc3ccccc3)ccc21
Reaction #1591331
title compound
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(cc1O)N(Cc1ccccc1)CCC2
Reaction #1623449
DOI: 10.1039/C8SC04228D
CN(C)CCC(O)c1ccc2c(c1)CCCN2C(=O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #1853201
3-[1-([4′-Chloro[1,1-biphenyl]-4-yl)carbonyl)-1,2,3,4-tetrahydro-6-quinolinyl]-3-hydroxy-N,N-dimethyl-1-propanamine
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #1855726
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc2c(c1)CCCN2Cc1ccccc1
Reaction #1898128
Compound 6
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter