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793498

O=C(O)c1ccc(CCN2CCC(Nc3ccc(Oc4ccc(Cl)cc4)cc3)CC2)cc1
Reaction #44802
4-[2-[4-[[4-(4-chlorophenoxy)phenyl]amino]-1-piperidinyl]ethyl]benzoic acid
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #55018
47
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC(N(C(=O)Cc2ccc(OC)cc2)c2ccc(Cl)cc2)CC1
Reaction #55020
ethyl 4-{N-(4-chlorophenyl)-N-[(4-methoxyphenyl)acetyl]amino}-1-piperidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #56411
47
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC(N(C(=O)Cc2ccc(OC)cc2)c2ccc(Cl)cc2)CC1
Reaction #56413
ethyl 4-{N-(4-chlorophenyl)-N-[(4-methoxyphenyl)acetyl]amino}-1-piperidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Nc2cccc(F)c2)CC1
Reaction #71617
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Nc2ccc(C(F)(F)F)cc2)CC1
Reaction #71627
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Nc2cccc(F)c2)CC1
Reaction #71637
1,1-Dimethylethyl 4-[(3-fluorophenyl)amino]-1-piperidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@@H]2[C@@H](C1)c1ccccc1N2c1ccccc1.Cl
Reaction #74959
pale greenish-white powder
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCN1CC[C@H]2[C@@H](C1)c1cccc3c1N2CCS3)c1ccc(F)cc1
Reaction #79323
4-((6bR,10aS)-1,2,6b,9,10,10a-hexahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indol-8(7H)-yl)-1-(4-fluorophenyl)-1-butanone
Ausbeute 31.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCN(c2ccccc2)C12CCNCC2
Reaction #81437
1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCc2ccccc2N1C1CCN(CC(O)c2ccc3c(c2)OCO3)CC1
Reaction #95352
desired product
Ausbeute 64.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(=O)CC[C@@]3(O)[C@H]1C5.CCC(=O)N(c1ccccc1)C1CCN(CCc2ccccc2)CC1
Reaction #155376
Naloxone Fentanyl
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(=O)CC[C@@]3(O)[C@H]1C5.CCC(=O)N(c1ccccc1)C1CCN(CCc2ccccc2)CC1
Reaction #155377
Naloxone Fentanyl
DOI: 10.6084/m9.figshare.5104873.v1
O[C@]12CCCC[C@H]1N(Cc1ccccc1)CC[C@H]2Nc1ccccc1
Reaction #160795
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O[C@]12CCCC[C@@H]1NCCC2Nc1ccccc1
Reaction #160796
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(=O)N1CCC(Nc2ccccc2)[C@@]2(O)CCCC[C@H]12
Reaction #160797
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1cc(N2CCN3CCC2CC3)ccc1[N+](=O)[O-]
Reaction #164565
5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-N-methyl-2-nitrobenzenesulfonamide
Ausbeute 80.6%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1cc(N2CCN3CCC2CC3)ccc1N
Reaction #164566
2-amino-5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-N-methylbenzenesulfonamide
Ausbeute 95.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CC2(CCN(Cc3ccccc3)CC2)N1c1ccccc1
Reaction #176159
DOI: 10.1039/C8SC04228D
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