dicyclohexyl-[3,6-dimethoxy-2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane

c1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1
Reaction #634
Ausbeute 6.3%750 AstraZeneca ELN dataset
c1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1
Reaction #637
Ausbeute 36.9%750 AstraZeneca ELN dataset
c1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1
Reaction #638
Ausbeute 42.0%750 AstraZeneca ELN dataset
c1ccc(Nc2ncco2)nc1
Reaction #674
Ausbeute 0.0%750 AstraZeneca ELN dataset
CNc1cc(Nc2ccccc2[N+](=O)[O-])ncn1
Reaction #86405
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cc(OC)c(Cl)c(N(COCC[Si](C)(C)C)C(=O)N(C)c2cc(Nc3ccc(N4CCN(C(=O)OC(C)(C)C)CC4)cc3[N+](=O)[O-])ncn2)c1Cl
Reaction #86480
title compound
Ausbeute 45.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1c(F)cncc1-c1cc2cnc(NC(=O)OC(C)(C)C)cc2c[n+]1[O-]
Reaction #556137
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
Cc1c(F)cncc1-c1cc2cnc(NC(=O)C3CC3)cc2c[n+]1[O-]
Reaction #556143
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CN1CCN(S(=O)(=O)C2CCN(c3c(N)cncc3F)CC2)CC1
Reaction #612088
5-fluoro-4-(4-((4-methylpiperazin-1-yl)sulfonyl)piperidin-1-yl)pyridin-3-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CN1CC=C(c2c(F)cncc2NC(=O)OC(C)(C)C)CC1
Reaction #612134
tert-butyl (5-fluoro-1′-methyl-1′,2′,3′,6′-tetrahydro-[4,4′-bipyridin]-3-yl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(C)(C)OC(=O)Nc1cncc(F)c1C1=CCN(C2COC2)CC1
Reaction #612140
tert-butyl (5-fluoro-1′-(oxetan-3-yl)-1′,2′,3′,6′-tetrahydro-[4,4′-bipyridin]-3-yl)carbamate
Ausbeute 24.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(C)(C)Nc1nccc2ccc(C(=O)O)cc12
Reaction #624383
1-(tert-butylamino)isoquinoline-7-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
COc1nn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c2cc(NC(=O)N[C@H](C)c3ccccc3)ncc12
Reaction #675358
(R)-1-(3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COC[C@@H](NC(=O)Nc1cc2c(cn1)c(OC)nn2C(c1ccccc1)(c1ccccc1)c1ccccc1)c1ccccc1
Reaction #675360
(S)-1-(2-methoxy-1-phenylethyl)-3-(3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COc1n[nH]c2cc(NC(=O)N[C@@H]3CN(C)C[C@H]3c3ccccc3)ncc12
Reaction #675366
1-(3-methoxy-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-[(3S,4R)-1-methyl-4-phenylpyrrolidin-3-yl]urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COCc1nc(NC(=O)N[C@H](C)c2ccccc2)cc2[nH]nc(OC)c12
Reaction #675373
(R)-1-(3-methoxy-4-(methoxymethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
C[C@@H](NC(=O)Nc1cc2[nH]nc(S(C)(=O)=O)c2cn1)c1ccccc1
Reaction #675377
(R)-1-(3-(methylsulfonyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cn1ccc2ccnc(N[C@@H]3CCCN(C(=O)OC(C)(C)C)C3)c21
Reaction #675542
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CNc1nn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c2cc(NC(=O)N[C@H](C)c3ccc(F)cc3)ncc12
Reaction #677976
(R)-1-(1-(4-fluorophenyl)ethyl)-3-(3-(methylamino)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCNc1nn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c2cc(NC(=O)N[C@H](C)c3ccccc3)ncc12
Reaction #677979
(R)-1-(3-(ethylamino)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
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