Ähnlichkeitssuche

12484

CC(C)(Cc1c[nH]c2c(C=CS(C)(=O)=O)cccc12)NC(=O)OC(C)(C)C
Reaction #8204
{2-[7-(2-Methanesulfonyl-vinyl)-1H-indol-3-yl)-1,1-dimethyl-ethyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2cnc3cc(Br)ccc3c2n1CC(C)(C)OCCS(C)(=O)=O
Reaction #9509
7-bromo-2-ethoxymethyl-1-{2-[2-(methanesulfonyl)ethoxy]-2-methylpropyl}-1H-imidazo[4,5-c]quinoline
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc2c(ncn2CCS(C)(=O)=O)c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60280
pure desired product
Ausbeute 59.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)c3c(C=CS(C)(=O)=O)ccc(N4CCN([C@H](C)c5ccccc5)CC4)c3C2=O)cc1OC
Reaction #70603
Compound 62
Ausbeute 19.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2cnc3ccccc3c2n1CC1(OCCS(C)(=O)=O)CCN(C(=O)OC(C)(C)C)CC1
Reaction #73007
tert-butyl 4-{[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}-4-[2-(methylsulfonyl)ethoxy]piperidine-1-carboxylate
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CCN1CCC(Oc2c(C#N)ncc3c2c2cc(Br)cnc2n3S(=O)(=O)c2ccccc2)CC1
Reaction #88604
title compound
Ausbeute 92.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc2c(c1)CCN(c1ccc(N3CC[C@@H](N(C)CCS(C)(=O)=O)C3)c(F)c1)C2=O
Reaction #156592
6-Butoxy-2-(3-fluoro-4-{(R)-3-[(2-methanesulfonylethyl)methylamino]pyrrolidin-1-yl}phenyl)-3,4-dihydro-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CCN1CCCN(c2ccc([N+](=O)[O-])cc2)CC1
Reaction #159390
1-(2-Methanesulfonyl-ethyl)-4-(4-nitro-phenyl)-[1,4]diazepane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cn(C[C@H]2CCCO2)/c(=N/C(=O)c2cc(C(F)(F)F)ccc2/C=C/S(C)(=O)=O)s1
Reaction #165733
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #172798
solid
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Oc1cc(-n2cnc3cc(-c4cnn(C)c4)ccc32)sc1C(N)=O)c1ccc(F)c(OC2CCN(CCS(C)(=O)=O)CC2)c1Cl
Reaction #175262
DOI: 10.1039/C8SC04228D
COc1cc(N2CCN(CCS(C)(=O)=O)CC2)c(C)cc1[N+](=O)[O-]
Reaction #183245
DOI: 10.1039/C8SC04228D
CS(=O)(=O)CCN1CC(c2cc(F)ccc2F)=CC1c1ccccc1
Reaction #189161
DOI: 10.1039/C8SC04228D
CCc1nc2ccccc2n1-c1nc(N2CCOCC2)c2nc(C3(OC)CN(CCS(C)(=O)=O)C3)n(C)c2n1
Reaction #195336
DOI: 10.1039/C8SC04228D
CCOCc1nc2cnc3ccccc3c2n1CC1(OCCS(C)(=O)=O)CCCC1
Reaction #198050
DOI: 10.1039/C8SC04228D
Cc1cc(OC2CCN(CCS(C)(=O)=O)CC2)ccc1Nc1nccc(-c2c(-c3cccc(C(=O)Nc4c(F)cccc4F)c3)nc3ccccn23)n1
Reaction #202421
DOI: 10.1039/C8SC04228D
COc1cc2c(=O)n(COC(=O)C(C)(C)C)cnc2cc1OCC1CCN(CCS(C)(=O)=O)CC1
Reaction #202479
DOI: 10.1039/C8SC04228D
CCNC(=O)Nc1ccc(-c2nc3c(c(N4CCOCC4C)n2)CCN(CCS(C)(=O)=O)C3)cc1
Reaction #221195
DOI: 10.1039/C8SC04228D
Cc1cc(C)c(CNC(=O)c2cc(C3=CCN(C4CCN(CCS(C)(=O)=O)CC4)CC3)nc3c2cnn3C(C)C)c(=O)[nH]1
Reaction #221282
DOI: 10.1039/C8SC04228D
CC1(C)CCC(C)(C)c2cc(C=CS(C)(=O)=O)c(C=O)cc21
Reaction #229035
DOI: 10.1039/C8SC04228D
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