An 58 Reaktionen beteiligt

761071

Ic1nc(-c2ccccc2)nc2ccccc12
Reaction #72715
4-Iodo-2-phenylquinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOc1cc(CN2CCC(Nc3nc(-c4ccccc4)nc4ccccc34)CC2)ccc1OC
Reaction #173276
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1C(=O)CCC2(C)c3ccc(Sc4nc(-c5ccccc5)nc5ccccc45)cc3CCC12
Reaction #174695
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccccc1OC1CCN(c2nc(-c3ccccc3)nc3ccccc23)C1
Reaction #255040
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(-c2nc(N3CCN(c4ccccn4)CC3)c3ccccc3n2)cc1
Reaction #275827
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCn1c(-c2ccc(Nc3nc(-c4ccccc4)nc4ccccc34)cc2)c(C#N)c2ccc(OC)cc21
Reaction #339769
1-ethyl-6-methoxy-2-[4-(2-phenylquinazolin-4-ylamino)-phenyl]-1H-indole-3-carbonitrile
Ausbeute 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CN1CC[C@]23CCCC[C@H]2[C@H]1Cc1ccc(Oc2nc(-c4ccccc4)nc4ccccc24)cc13
Reaction #343756
product
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
OC1CCN(c2nc(-c3ccccc3)nc3ccccc23)CC1
Reaction #441974
title compound
Ausbeute 41.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
O.OC1CCN(c2nc(-c3ccccc3)nc3ccccc23)C1.OC1CCN(c2nc(-c3ccccc3)nc3ccccc23)C1
Reaction #441975
title compound
Ausbeute 72.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
CC(C)(CO)Nc1nc(-c2ccccc2)nc2ccccc12
Reaction #441976
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
OCC1CCCN(c2nc(-c3ccccc3)nc3ccccc23)C1
Reaction #441977
title compound
Ausbeute 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
COc1ccccc1OC1CCN(c2nc(-c3ccccc3)nc3ccccc23)C1
Reaction #441978
4-[3-(2-Methoxyphenoxy)-1-pyrrolidinyl]-2-phenylquinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
c1ccc(-c2nc(N3CCN(c4ccccn4)CC3)c3ccccc3n2)cc1
Reaction #441979
2-Phenyl-4-[4-(2-pyridinyl)-1-piperazinyl]quinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
COc1ccccc1OCC(O)CNc1nc(-c2ccccc2)nc2ccccc12.O
Reaction #441980
title compound
Ausbeute 28.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
COC(=O)c1ccccc1-c1ccc([CH2][Zn+])cc1.[Br-]
Reaction #486178
[[2'-(methoxycarbonyl)(1,1'-biphenyl)-4-yl]-methyl]zinc bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CCn1c(-c2ccc(Nc3nc(-c4ccccc4)nc4ccccc34)cc2)c(C#N)c2ccc(OC)cc21
Reaction #589397
1-ethyl-6-methoxy-2-[4-(2-phenylquinazolin-4-ylamino)-phenyl]-1H-indole-3-carbonitrile
Ausbeute 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CCn1c(-c2ccc(Nc3nc(-c4ccccc4)nc4ccccc34)cc2)c(C#N)c2ccc(OC)cc21
Reaction #593279
1-ethyl-6-methoxy-2-[4-(2-phenylquinazolin-4-ylamino)-phenyl]-1H-indole-3-carbonitrile
Ausbeute 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COC(=O)c1ccccc1-c1ccc([CH2][Zn+])cc1.[Br-]
Reaction #699622
[[2'-(methoxycarbonyl)(1,1'-biphenyl)-4-yl]-methyl] zinc bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
c1ccc(-c2nc(Nc3ccncc3)c3ccccc3n2)cc1
Reaction #721803
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
COc1cccc(Nc2nc(-c3ccccc3)nc3ccccc23)c1
Reaction #721805
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
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