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779023

CC(C)(C)OC(=O)N1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2Cl)CC1
Reaction #60678
4-{2-[(3-Chloro-1H-indole-6-carbonyl)amino]-2-(2-chloro-phenyl)ethoxymethyl}piperidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(COC[C@H](NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2)CC1.Cl
Reaction #60695
3-Chloro-N-[(R)-1-phenyl-2-(1-isopropylpiperidin-4-yl-methoxy)ethyl]-1H-indole-6-carboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](COCC1CCN(C2CCCC2)CC1)c1ccccc1)c1ccc2c(Cl)c[nH]c2c1
Reaction #60696
3-Chloro-N-[(R)-1-phenyl-2-(1-cyclopentylpiperidin-4-yl-methoxy)ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(COC[C@H](NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2)CC1
Reaction #60697
3-Chloro-N-[(R)-1-phenyl-2-(1-methylpiperidin-4-yl-methoxy)ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@@H](COCC1CCN(C2CC2)CC1)c1ccccc1)c1ccc2c(Cl)c[nH]c2c1
Reaction #60698
3-Chloro-N-[(R)-1-phenyl-2-(1-cyclopropylpiperidin-4-yl-methoxy)ethyl]-1H-indole-6-carboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2Cl)CC1
Reaction #60701
3-Chloro-N-[1-(2-chlorophenyl)-2-(1-isopropylpiperidin-4-yl-methoxy)ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2Cl)CC1
Reaction #60702
3-Chloro-N-[1-(2-chlorophenyl)-2-(1-methylpiperidin-4-yl-methoxy)ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2Cl)CC1
Reaction #60703
3-Chloro-N-[1-(2-chlorophenyl)-2-(1-ethylpiperidin-4-yl-methoxy)ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(COCC1CCN(CCF)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #60704
title compound
Ausbeute 32.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(COCC1CCN(C(=O)C(F)(F)F)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #60705
title compound
Ausbeute 42.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(COCC1CCN(CC(F)(F)F)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #60706
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(COCC1CCN(CCO)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #60707
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(COCC1CCN(CCF)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #211690
DOI: 10.1039/C8SC04228D
O=C(NC(COCC1CCN(CC(F)(F)F)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #270775
DOI: 10.1039/C8SC04228D
O=C(NC(COCC1CCN(C(=O)C(F)(F)F)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #1037243
DOI: 10.1039/C8SC04228D
CC(C)N1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2Cl)CC1
Reaction #1643542
DOI: 10.1039/C8SC04228D
CCN1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2Cl)CC1
Reaction #1650209
DOI: 10.1039/C8SC04228D
O=C(NC(COCC1CCN(CCO)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #2220472
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2Cl)CC1
Reaction #2416703
DOI: 10.1039/C8SC04228D