Ähnlichkeitssuche

13895

COCCc1nc2c(N)nc3cc(Br)ccc3c2n1CC(C)C
Reaction #9481
7-Bromo-2-(2-methoxyethyl)-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #9488
tert-butyl 4-{[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}piperidine-1-carboxylate
Ausbeute 85.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CC(C)(C)OCCS(C)(=O)=O
Reaction #9510
2-ethoxymethyl-1-{2-[2-(methanesulfonyl)ethoxy]-2-methylpropyl}-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine
Ausbeute 58.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CCCC(C)S(N)(=O)=O
Reaction #9521
methyl 4-[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]butane-1-sulfonamide
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #9538
tert-butyl 4-{[4-amino-2-ethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}piperidine-1-carboxylate
Ausbeute 59.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CCN1CCNCC1
Reaction #9542
2-ethoxymethyl-1-(2-piperazin-1-ylethyl)-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine
Ausbeute 78.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1C[C@H]1COC(C)(C)O1
Reaction #9582
(S)-1-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine
Ausbeute 54.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CC1CCCCN1C(=O)OC(C)(C)C
Reaction #9583
tert-butyl 2-{[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}piperidine-1-carboxylate
Ausbeute 70.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1Cc1ccc(CNC(=O)OC(C)(C)C)cc1
Reaction #9589
tert-butyl{4-[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-ylmethyl]benzyl}carbamate
Ausbeute 64.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(C(=O)C2CCCCC2)cc(-c2cccnc2)cc1[N+](=O)[O-]
Reaction #40530
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(Br)c2oc(C(C)(C)C)nc2c1C#N
Reaction #45545
compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Br)c(-c2ccccc2)c(C)c(C#N)c1NC(=O)C(F)(F)F
Reaction #45573
compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Br)c(-c2ccccc2)c(C)c(C#N)c1NC(=O)C(F)(F)F
Reaction #183445
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(N)=O
Reaction #245785
DOI: 10.1039/C8SC04228D
COc1cc(Cl)ccc1Cc1cccnc1
Reaction #280615
DOI: 10.1039/C8SC04228D
Nc1ccc(-c2cccnc2)cc1[N+](=O)[O-]
Reaction #304326
title compound
Ausbeute 105.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(N)=O.NCCNS(=O)(=O)c1cc(-c2ccccc2)cc2cnccc12
Reaction #357177
7-phenyl-isoquinoline-5-sulfonic acid (2-amino-ethyl)-amide carbamic acid t-butyl ester
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)ccc1Cc1cccnc1
Reaction #359936
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)Cc2ccccc2-c2cccnc2)CC1
Reaction #391832
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccccc2CNC(=O)c2ccc(F)c(NC(=O)c3cnc4cc(-c5cccnc5)ccn34)c2)CC1
Reaction #422453
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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